6-AMINOPYRIDIN-3-YL THIAZOLES AS MODULATORS OF RORyT

ABSTRACT

The present invention comprises compounds of Formula I. 
     
       
         
         
             
             
         
       
         
         
           
             wherein: 
             A 1 , A 2 , A 3 , A 4 , A 5 , R 1 , and R 2  are defined in the specification. 
           
         
       
    
     The invention also comprises a method of treating or ameliorating a syndrome, disorder or disease, wherein the syndrome, disorder or disease is rheumatoid arthritis or psoriasis. The invention also comprises a method of modulating RORγt activity in a mammal by administration of a therapeutically effective amount of at least one compound of Formula I.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 15/497,565, filed on Apr. 26, 2017, which claims priority from U.S. Application No. 62/328,074, filed on Apr. 27, 2016, which are incorporated herein by reference.

FIELD OF THE INVENTION

The invention is directed to substituted thiazole compounds, which are modulators of the nuclear receptor RORγt, pharmaceutical compositions, and methods for use thereof. More particularly, the RORγt modulators are useful for preventing, treating or ameliorating an RORγt mediated inflammatory syndrome, disorder or disease.

BACKGROUND OF THE INVENTION

Retinoic acid-related nuclear receptor gamma t (RORγt) is a nuclear receptor, exclusively expressed in cells of the immune system, and a key transcription factor driving Th17 cell differentiation. Th17 cells are a subset of CD4+ T cells, expressing CCR6 on their surface to mediate their migration to sites of inflammation, and dependent on IL-23 stimulation, through the IL-23 receptor, for their maintenance and expansion. Th17 cells produce several proinflammatory cytokines including IL-17A, IL-17F, IL-21, and IL-22 (Korn, T., E. Bettelli, et al. (2009). “IL-17 and Th17 Cells.” Annu Rev Immunol 27: 485-517), which stimulate tissue cells to produce a panel of inflammatory chemokines, cytokines and metalloproteases, and promote recruitment of granulocytes (Kolls, J. K. and A. Linden (2004). “Interleukin-17 family members and inflammation.” Immunity 21(4): 467-76; Stamp, L. K., M. J. James, et al. (2004). “Interleukin-17: the missing link between T-cell accumulation and effector cell actions in rheumatoid arthritis” Immunol Cell Biol 82(1): 1-9). Th17 cells have been shown to be the major pathogenic population in several models of autoimmune inflammation, including collagen-induced arthritis (CIA) and experimental autoimmune encephalomyelitis (EAE) (Dong, C. (2006). “Diversification of T-helper-cell lineages: finding the family root of IL-17-producing cells.” Nat Rev Immunol 6(4): 329-33; McKenzie, B. S., R. A. Kastelein, et al. (2006). “Understanding the IL-23-IL-17 immune pathway.” Trends Immunol 27(1): 17-23). RORγt-deficient mice are healthy and reproduce normally, but have shown impaired Th17 cell differentiation in vitro, a significantly reduced Th17 cell population in vivo, and decreased susceptibility to EAE (Ivanov, II, B. S. McKenzie, et al. (2006). “The orphan nuclear receptor RORgammat directs the differentiation program of proinflammatory IL-17+T helper cells.” Cell 126(6): 1121-33). Mice deficient for IL-23, a cytokine required for Th17 cell survival, fail to produce Th17 cells and are resistant to EAE, CIA, and inflammatory bowel disease (IBD) (Cua, D. J., J. Sherlock, et al. (2003). “Interleukin-23 rather than interleukin-12 is the critical cytokine for autoimmune inflammation of the brain.” Nature 421(6924): 744-8; Langrish, C. L., Y. Chen, et al. (2005). “IL-23 drives a pathogenic T cell population that induces autoimmune inflammation.” J Exp Med 201(2): 233-40; Yen, D., J. Cheung, et al. (2006). “IL-23 is essential for T cell-mediated colitis and promotes inflammation via IL-17 and IL-6.” J Clin Invest 116(5): 1310-6). Consistent with these findings, an anti-IL23-specific monoclonal antibody blocks development of psoriasis-like inflammation in a murine disease model (Tonel, G., C. Conrad, et al. “Cutting edge: A critical functional role for IL-23 in psoriasis.” J Immunol 185(10): 5688-91).

RORγT deficient mice exhibited resistance to learned helplessness. Treatment with the RORγT inhibitor SR1001, or anti-interleukin-17A antibodies reduced Th17-dependent learned helplessness (Beurel, E., Harrington, L. E., Jope, R. S. (2013) “Inflammatory T helper 17 cells promote depression-like behavior in mice.” Biol Psychiatry 73(7): 622-30). In human patients with major depressive disorder, both peripheral blood lymphocyte RORγT mRNA expression and peripheral Th17 cells were found to be elevated relative to the control group (Chen, Y., et al. (2011). “Emerging tendency towards autoimmune process in major depressive patients: A novel insight from Th17 cells.” Psychiatry Research 188(2): 224-230).

Administration of RORγ inverse agonist SR1555 to obese diabetic mice resulted in a modest reduction in food intake accompanied with significant reduction in fat mass, resulting in reduced body weight and improved insulin sensitivity (Chang, M. R. et al. (2015) “Antiobesity Effect of a Small Molecule Repressor of RORγ.” Mol Pharmacol. 88(1): 48-56). In addition, Rorγ−/− mice are protected from hyperglycemia and insulin resistance in the state of obesity (Meissburger, B. et al. (2011) “Adipogenesis and insulin sensitivity in obesity are regulated by retinoid-related orphan receptor gamma.” EMBO Mol Med. 3(11): 637-651).

In humans, a number of observations support the role of the IL-23/Th17 pathway in the pathogenesis of inflammatory diseases. IL-17, the key cytokine produced by Th17 cells, is expressed at elevated levels in a variety of allergic and autoimmune diseases (Barczyk, A., W. Pierzchala, et al. (2003). “Interleukin-17 in sputum correlates with airway hyperresponsiveness to methacholine.” Respir Med 97(6): 726-33; Fujino, S., A. Andoh, et al. (2003). “Increased expression of interleukin 17 in inflammatory bowel disease.” Gut 52(1): 65-70; Lock, C., G. Hermans, et al. (2002). “Gene-microarray analysis of multiple sclerosis lesions yields new targets validated in autoimmune encephalomyelitis.” Nat Med 8(5): 500-8; Krueger, J. G., S. Fretzin, et al. “IL-17A is essential for cell activation and inflammatory gene circuits in subjects with psoriasis.” J Allergy Clin Immunol 130(1): 145-154 e9). Furthermore, human genetic studies have shown association of polymorphisms in the genes for Th17 cell-surface receptors, IL-23R and CCR6, with susceptibility to IBD, multiple sclerosis (MS), rheumatoid arthritis (RA) and psoriasis (Gazouli, M., I. Pachoula, et al. “NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.” World J Gastroenterol 16(14): 1753-8, Nunez, C., B. Dema, et al. (2008). “IL23R: a susceptibility locus for celiac disease and multiple sclerosis?” Genes Immun 9(4): 289-93; Bowes, J. and A. Barton “The genetics of psoriatic arthritis: lessons from genome-wide association studies.” Discov Med 10(52): 177-83; Kochi, Y., Y. Okada, et al. “A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility.” Nat Genet 42(6): 515-9).

Ustekinumab (Stelara®), an anti-p40 monoclonal antibody blocking both IL-12 and IL-23, is approved for the treatment of adult patients (18 years or older), with moderate to severe plaque psoriasis, who are candidates for phototherapy or systemic therapy. Currently, monoclonal antibodies specifically targeting only IL-23, to more selectively inhibit the Th17 subset, are also in clinical development for psoriasis (Garber K. (2011). “Psoriasis: from bed to bench and back” Nat Biotech 29, 563-566), further implicating the important role of the IL-23- and RORγt-driven Th17 pathway in this disease. Results from recent phase II clinical studies strongly support this hypothesis, as anti-IL-17 receptor and anti-IL-17 therapeutic antibodies both demonstrated high levels of efficacy in patients with chronic psoriasis (Papp, K. A., “Brodalumab, an anti-interleukin-17-receptor antibody for psoriasis.” N Engl J Med 2012 366(13): 1181-9; Leonardi, C., R. Matheson, et al. “Anti-interleukin-17 monoclonal antibody ixekizumab in chronic plaque psoriasis.” N Engl J Med 366(13): 1190-9). Anti-IL-17 antibodies have also demonstrated clinically relevant responses in early trials in RA and uveitis (Hueber, W., Patel, D. D., Dryja, T., Wright, A. M., Koroleva, I, Bruin, G., Antoni, C., Draelos, Z., Gold, M. H., Durez, P., Tak, P. P., Gomez-Reino, J. J., Foster, C. S., Kim, R. Y., Samson, C. M., Falk, N. S., Chu, D. S., Callanan, D., Nguyen, Q. D., Rose, K., Haider, A., Di Padova, F. (2010) Effects of AIN457, a fully human antibody to interleukin-17A, on psoriasis, rheumatoid arthritis, and uveitis. Sci Transl Med 2, 5272).

All the above evidence supports inhibition of the Th17 pathway by modulating RORγt activity as an effective strategy for the treatment of immune-mediated inflammatory diseases.

SUMMARY OF THE INVENTION

The present invention comprises a compound of Formula I:

wherein

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, cyclopropyl, OCF₃, or OCHF₂;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, —OCHF₂, or OCF₃; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is H, —C₍₁₋₆₎alkyl,

—SO₂CH(CH₃)₂, —SO₂CH₃,

wherein said —C₍₁₋₆₎alkyl is optionally substituted with one —NH₂ group, one or two —OH groups, and may be additionally substituted with up to six fluorine atoms;

A⁴ is —H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₁₋₆₎alkyl,

wherein said —C₍₁₋₆₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms; and said —C₍₁₋₆₎alkyl is independently optionally substituted with one cyclobutyl, or up to two cyclopropyl groups; and pharmaceutically acceptable salts thereof.

DETAILED DESCRIPTION OF THE INVENTION

The present invention comprises a compound of Formula I:

wherein

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, cyclopropyl, OCF₃, or OCHF₂;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, —OCHF₂, or OCF₃; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is H, —C₍₁₋₆₎alkyl,

—SO₂CH(CH₃)₂, —SO₂CH₃,

wherein said —C₍₁₋₆₎alkyl is optionally substituted with one —NH₂ group, one or two —OH groups, and may be additionally substituted with up to six fluorine atoms;

A⁴ is —H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₁₋₆₎alkyl

wherein said —C₍₁₋₆₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms; and said —C₍₁₋₆₎alkyl is independently optionally substituted with one cyclobutyl, or up to two cyclopropyl groups; and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, cyclopropyl, OCF₃, or OCHF₂; R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, —OCHF₂, or OCF₃; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is H, —C₍₁₋₆₎alkyl,

—SO₂CH(CH₃)₂, —SO₂CH₃,

wherein said —C₍₁₋₆₎alkyl is optionally substituted with one —N₂ group, one or two —OH groups, and may be additionally substituted with up to six fluorine atoms;

A⁴ is —H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₆₎alkyl,

wherein said —C₍₃₋₆₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, or cyclopropyl;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, or —OCHF₂; provided that R² may not be H if R is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is H, —C₍₁₋₆₎alkyl,

—SO₂CH(CH₃)₂, —SO₂CH₃,

wherein said —C₍₁₋₆₎alkyl is optionally substituted with one —NH₂ group, one or two —OH groups, and may be additionally substituted with up to six fluorine atoms;

A⁴ is —H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₆₎alkyl,

wherein said —C₍₃₋₆₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, or cyclopropyl;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, or —OCHF₂; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is H, —C₍₁₋₆₎alkyl,

—SO₂CH(CH₃)₂, —SO2CH₃,

wherein said —C₍₁₋₆₎alkyl is optionally substituted with one —NH₂ group, one or two —OH groups, and may be additionally substituted with up to six fluorine atoms;

A⁴ is H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₆₎alkyl

wherein said —C₍₃₋₆₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, or cyclopropyl;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, or —OCHF₂; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is H, —C₍₁₋₆₎alkyl,

—SO₂CH(CH₃)₂, —SO₂CH₃,

wherein said —C₍₁₋₆₎alkyl is optionally substituted with one —NH₂ group, one or two —OH groups, and may be additionally substituted with up to six fluorine atoms;

A⁴ is H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₆₎alkyl,

wherein said —C₍₃₋₆₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, cyclopropyl, OCF₃, or OCHF₂;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, —OCHF₂, or OCF₃; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is C₍₄₋₆₎alkyl,

wherein said C₍₄₋₆₎alkyl is optionally substituted with one —OH group;

A⁴ is —H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A is —C₍₄₋₆₎cycloalkyl, —C₍₂₋₅₎alkyl,

wherein said —C₍₂₋₅₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms; and said —C₍₂₋₅₎alkyl is independently optionally substituted with up to two cyclopropyl groups;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, cyclopropyl, OCF₃, or OCHF₂;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, —OCHF₂, or OCF₃; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is C₍₄₋₅₎alkyl,

wherein said C₍₄₋₅₎alkyl is optionally substituted with one —OH group;

A⁴ is —H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₅₎alkyl,

wherein said —C₍₃₋₅₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, cyclopropyl, OCF₃, or OCHF₂;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, —OCHF₂, or OCF₃; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is —CH₂C(CH₃)₂OH, —CH₂CH₂C(CH₃)₂OH,

—CH(CH₃)C(CH₃)₂OH, or —C(CH₃)₂CH₂OH;

A⁴ is —H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₅₎alkyl,

wherein said —C₍₃₋₅₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, or cyclopropyl; R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, or —OCHF₂; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is —CH₂C(CH₃)₂OH, —CH₂CH₂C(CH₃)₂OH,

—CH(CH₃)C(CH₃)₂OH, or —C(CH₃)₂CH₂OH;

A⁴ is —H, or —CH₃;

or A³ and A⁴ may be taken together with their attached nitrogen to form a ring selected from the group consisting of

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₅₎alkyl,

wherein said —C₍₃₋₅₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, or cyclopropyl;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, or —OCHF₂; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is —CH₂C(CH₃)₂OH, —CH₂CH₂C(CH₃)₂OH,

A⁴ is H;

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₅₎alkyl,

wherein said —C₍₃₋₅₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, or cyclopropyl;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, or —OCHF₂; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring selected from the group consisting of

A³ is —CH₂C(CH₃)₂OH, —CH₂CH₂C(CH₃)₂H,

A⁴ is H;

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₅₎alkyl,

wherein said —C₍₃₋₅₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

In another embodiment of the invention:

R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, or cyclopropyl;

R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, or —OCHF₂; provided that R² may not be H if R¹ is H;

A¹ and A² are taken together with their attached nitrogen to form a ring which is

A³ is —CH₂C(CH₃)₂OH, —CH₂CH₂C(CH₃)₂OH,

A⁴ is H;

A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₅₎alkyl,

wherein said —C₍₃₋₅₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms;

and pharmaceutically acceptable salts thereof.

Another embodiment of the invention is a compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

Another embodiment of the invention is a compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

Another embodiment of the invention is a compound selected from the group consisting of:

Another embodiment of the invention is a compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

Another embodiment of the invention is a compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

Another embodiment of the invention is a compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

Another embodiment of the invention is a compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

Another embodiment of the invention is a compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

Another embodiment of the invention is a compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

Another embodiment of the invention comprises a compound of Formula I and a pharmaceutically acceptable carrier.

The present invention also provides a method for preventing, treating or ameliorating an RORγt mediated inflammatory syndrome, disorder or disease comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of preventing, treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is selected from the group consisting of: ophthalmic disorders, uveitis, atherosclerosis, rheumatoid arthritis, psoriasis, psoriatic arthritis, atopic dermatitis, multiple sclerosis, Crohn's Disease, ulcerative colitis, ankylosing spondylitis, nephritis, organ allograft rejection, fibroid lung, systic fibrosis, renal insufficiency, diabetes and diabetic complications, diabetic nephropathy, diabetic retinopathy, diabetic retinitis, diabetic microangiopathy, tuberculosis, chronic obstructive pulmonary disease, sarcoidosis, invasive staphylococcia, inflammation after cataract surgery, allergic rhinitis, allergic conjunctivitis, chronic urticaria, systemic lupus erythematosus, asthma, allergic asthma, steroid resistant asthma, neutrophilic asthma, periodontal diseases, periodonitis, gingivitis, gum disease, diastolic cardiomyopathies, cardiac infarction, myocarditis, chronic heart failure, angiostenosis, restenosis, reperfusion disorders, glomerulonephritis, solid tumors and cancers, chronic lymphocytic leukemia, chronic myelocytic leukemia, multiple myeloma, malignant myeloma, Hodgkin's disease, carcinomas of the bladder, breast, cervix, colon, lung, prostate, or stomach, depression and metabolic syndrome comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is selected from the group consisting of: rheumatoid arthritis, psoriasis, chronic obstructive pulmonary disorder, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, and ulcerative colitis.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is selected from the group consisting of: depression and metabolic syndrome.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is selected from the group consisting of: rheumatoid arthritis, psoriasis, chronic obstructive pulmonary disorder, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, and ulcerative colitis comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is selected from the group consisting of: inflammatory bowel diseases, rheumatoid arthritis, psoriasis, chronic obstructive pulmonary disorder, psoriatic arthritis, ankylosing spondylitis, neutrophilic asthma, steroid resistant asthma, multiple sclerosis, and systemic lupus erythematosus comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is selected from the group consisting of: inflammatory bowel diseases, rheumatoid arthritis, psoriasis, chronic obstructive pulmonary disorder, psoriatic arthritis, ankylosing spondylitis, neutrophilic asthma, steroid resistant asthma, multiple sclerosis, systemic lupus erythematosus, depression and metabolic syndrome comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is selected from the group consisting of: rheumatoid arthritis, and psoriasis comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is selected from the group consisting of: psoriatic arthritis and psoriasis comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is selected from the group consisting of: depression and metabolic syndrome comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, in a subject in need thereof comprising administering to the subject an effective amount of the compound of Formula I or composition or medicament thereof in a combination therapy with one or more anti-inflammatory agents, or immunosuppressive agents, wherein said syndrome, disorder or disease is selected from the group consisting of: rheumatoid arthritis, and psoriasis.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, in a subject in need thereof comprising administering to the subject an effective amount of the compound of Formula I or composition or medicament thereof in a combination therapy with one or more anti-inflammatory agents, or immunosuppressive agents, wherein said syndrome, disorder or disease is selected from the group consisting of: psoriatic arthritis and psoriasis.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, in a subject in need thereof comprising administering to the subject an effective amount of the compound of Formula I or composition or medicament thereof in a combination therapy with one or more anti-inflammatory agents, or immunosuppressive agents, wherein said syndrome, disorder or disease is selected from the group consisting of: depression and metabolic syndrome.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is rheumatoid arthritis, comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is psoriasis comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is chronic obstructive pulmonary disorder comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is psoriatic arthritis comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is ankylosing spondylitis comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating an inflammatory bowel disease, wherein said inflammatory bowel disease is Crohn's disease comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating an inflammatory bowel disease, wherein said inflammatory bowel disease is ulcerative colitis comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is neutrophilic asthma comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is steroid resistant asthma comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is multiple sclerosis comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is systemic lupus erythematosus comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is depression comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The present invention provides a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is metabolic syndrome comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

The invention also relates to methods of modulating RORγt activity in a mammal by administration of an effective amount of at least one compound of Formula I.

Another embodiment of the invention is a method of inhibiting production of interleukin-17, comprising administering to a subject in need thereof an effective amount of a compound of Formula I.

Definitions

The term “administering” with respect to the methods of the invention, means a method for therapeutically or prophylactically preventing, treating or ameliorating a syndrome, disorder or disease as described herein by using a compound of Formula I or a form, composition or medicament thereof. Such methods include administering an effective amount of said compound, compound form, composition or medicament at different times during the course of a therapy or concurrently in a combination form. The methods of the invention are to be understood as embracing all known therapeutic treatment regimens.

The term “subject” refers to a patient, which may be an animal, typically a mammal, typically a human, which has been the object of treatment, observation or experiment and is at risk of (or susceptible to) developing a syndrome, disorder or disease that is associated with abberant RORγt expression or RORγt overexpression, or a patient with an inflammatory condition that accompanies syndromes, disorders or diseases associated with abberant RORγt expression or RORγt overexpression.

The term “effective amount” means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue system, animal or human, that is being sought by a researcher, veterinarian, medical doctor, or other clinician, which includes preventing, treating or ameliorating the symptoms of a syndrome, disorder or disease being treated.

As used herein, the term “composition” is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combinations of the specified ingredients in the specified amounts.

The term “alkyl” refers to both linear and branched chain radicals of up to 12 carbon atoms, preferably up to 6 carbon atoms, unless otherwise indicated, and includes, but is not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, hexyl, isohexyl, heptyl, octyl, 2,2,4-trimethylpentyl, nonyl, decyl, undecyl and dodecyl. Any alkyl group may be optionally substituted with one OCH₃, one OH, or up to two fluorine atoms.

The term “C_((a-b))” (where a and b are integers referring to a designated number of carbon atoms) refers to an alkyl, alkenyl, alkynyl, alkoxy or cycloalkyl radical or to the alkyl portion of a radical in which alkyl appears as the prefix root containing from a to b carbon atoms inclusive. For example, C₍₁₋₄₎ denotes a radical containing 1, 2, 3 or 4 carbon atoms.

Pharmaceutically Acceptable Salts

Pharmaceutically acceptable acidic/anionic salts include, and are not limited to acetate, benzenesulfonate, benzoate, bicarbonate, bitartrate, bromide, calcium edetate, camsylate, carbonate, chloride, citrate, dihydrochloride, edetate, edisylate, estolate, esylate, fumarate, glyceptate, gluconate, glutamate, glycollylarsanilate, hexylresorcinate, hydrabamine, hydrobromide, hydrochloride, hydroxynaphthoate, iodide, isethionate, lactate, lactobionate, malate, maleate, mandelate, mesylate, methylbromide, methylnitrate, methylsulfate, mucate, napsylate, nitrate, pamoate, pantothenate, phosphate/diphosphate, polygalacturonate, salicylate, stearate, subacetate, succinate, sulfate, tannate, tartrate, teoclate, tosylate and triethiodide. Organic or inorganic acids also include, and are not limited to, hydriodic, perchloric, sulfuric, phosphoric, propionic, glycolic, methanesulfonic, hydroxyethanesulfonic, oxalic, 2-naphthalenesulfonic, p-toluenesulfonic, cyclohexanesulfamic, saccharinic or trifluoroacetic acid.

Pharmaceutically acceptable basic/cationic salts include, and are not limited to aluminum, 2-amino-2-hydroxymethyl-propane-1,3-diol (also known as tris(hydroxymethyl)aminomethane, tromethane or “TRIS”), ammonia, benzathine, t-butylamine, calcium, calcium gluconate, calcium hydroxide, chloroprocaine, choline, choline bicarbonate, choline chloride, cyclohexylamine, diethanolamine, ethylenediamine, lithium, LiOMe, L-lysine, magnesium, meglumine, NH₃, NH₄OH, N-methyl-D-glucamine, piperidine, potassium, potassium-t-butoxide, potassium hydroxide (aqueous), procaine, quinine, sodium, sodium carbonate, sodium-2-ethylhexanoate, sodium hydroxide, triethanolamine, or zinc.

Methods of Use

The present invention is directed to a method for preventing, treating or ameliorating a RORγt mediated inflammatory syndrome, disorder or disease comprising administering to a subject in need thereof an effective amount of a compound of Formula I or a form, composition or medicament thereof.

Since RORγt is an N-terminal isoform of RORγ, it is recognized that compounds of the present invention which are modulators of RORγt are likely to be modulators of RORγ as well. Therefore the mechanistic description “RORγt modulators” is intended to encompass RORγ modulators as well.

When employed as RORγt modulators, the compounds of the invention may be administered in an effective amount within the dosage range of about 0.5 mg to about 10 g, preferably between about 0.5 mg to about 5 g, in single or divided daily doses. The dosage administered will be affected by factors such as the route of administration, the health, weight and age of the recipient, the frequency of the treatment and the presence of concurrent and unrelated treatments.

It is also apparent to one skilled in the art that the therapeutically effective dose for compounds of the present invention or a pharmaceutical composition thereof will vary according to the desired effect. Therefore, optimal dosages to be administered may be readily determined by one skilled in the art and will vary with the particular compound used, the mode of administration, the strength of the preparation, and the advancement of the disease condition. In addition, factors associated with the particular subject being treated, including subject age, weight, diet and time of administration, will result in the need to adjust the dose to an appropriate therapeutic level. The above dosages are thus exemplary of the average case. There can, of course, be individual instances where higher or lower dosage ranges are merited, and such are within the scope of this invention.

The compounds of Formula I may be formulated into pharmaceutical compositions comprising any known pharmaceutically acceptable carriers. Exemplary carriers include, but are not limited to, any suitable solvents, dispersion media, coatings, antibacterial and antifungal agents and isotonic agents. Exemplary excipients that may also be components of the formulation include fillers, binders, disintegrating agents and lubricants.

The pharmaceutically-acceptable salts of the compounds of Formula I include the conventional non-toxic salts or the quaternary ammonium salts which are formed from inorganic or organic acids or bases. Examples of such acid addition salts include acetate, adipate, benzoate, benzenesulfonate, citrate, camphorate, dodecylsulfate, hydrochloride, hydrobromide, lactate, maleate, methanesulfonate, nitrate, oxalate, pivalate, propionate, succinate, sulfate and tartrate. Base salts include ammonium salts, alkali metal salts such as sodium and potassium salts, alkaline earth metal salts such as calcium and magnesium salts, salts with organic bases such as dicyclohexylamino salts and salts with amino acids such as arginine. Also, the basic nitrogen-containing groups may be quaternized with, for example, alkyl halides.

The pharmaceutical compositions of the invention may be administered by any means that accomplish their intended purpose. Examples include administration by parenteral, subcutaneous, intravenous, intramuscular, intraperitoneal, transdermal, buccal or ocular routes. Alternatively or concurrently, administration may be by the oral route. Suitable formulations for parenteral administration include aqueous solutions of the active compounds in water-soluble form, for example, water-soluble salts, acidic solutions, alkaline solutions, dextrose-water solutions, isotonic carbohydrate solutions and cyclodextrin inclusion complexes.

The present invention also encompasses a method of making a pharmaceutical composition comprising mixing a pharmaceutically acceptable carrier with any of the compounds of the present invention. Additionally, the present invention includes pharmaceutical compositions made by mixing a pharmaceutically acceptable carrier with any of the compounds of the present invention.

Polymorphs and Solvates

Furthermore, the compounds of the present invention may have one or more polymorph or amorphous crystalline forms and as such are intended to be included in the scope of the invention. In addition, the compounds may form solvates, for example with water (i.e., hydrates) or common organic solvents. As used herein, the term “solvate” means a physical association of the compounds of the present invention with one or more solvent molecules. This physical association involves varying degrees of ionic and covalent bonding, including hydrogen bonding. In certain instances the solvate will be capable of isolation, for example when one or more solvent molecules are incorporated in the crystal lattice of the crystalline solid. The term “solvate” is intended to encompass both solution-phase and isolatable solvates. Non-limiting examples of suitable solvates include ethanolates, methanolates, and the like.

It is intended that the present invention include within its scope polymorphs and solvates of the compounds of the present invention. Thus, in the methods of treatment of the present invention, the term “administering” shall encompass the means for treating, ameliorating or preventing a syndrome, disorder or disease described herein with the compounds of the present invention or a polymorph or solvate thereof, which would obviously be included within the scope of the invention albeit not specifically disclosed.

In another embodiment, the invention relates to a compound as described in Formula I for use as a medicament.

In another embodiment, the invention relates to the use of a compound as described in Formula I for the preparation of a medicament for the treatment of a disease associated with an elevated or aberrant RORγt activity.

The present invention includes within its scope prodrugs of the compounds of this invention. In general, such prodrugs will be functional derivatives of the compounds which are readily convertible in vivo into the required compound. Thus, in the methods of treatment of the present invention, the term “administering” shall encompass the treatment of the various disorders described with the compound specifically disclosed or with a compound which may not be specifically disclosed, but which converts to the specified compound in vivo after administration to the patient. Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in “Design of Prodrugs”, Ed. H. Bundgaard, Elsevier, 1985.

Furthermore, it is intended that within the scope of the present invention, any element, in particular when mentioned in relation to a compound of Formula I, shall comprise all isotopes and isotopic mixtures of said element, either naturally occurring or synthetically produced, either with natural abundance or in an isotopically enriched form. For example, a reference to hydrogen includes within its scope ¹H, ²H (D), and ³H (T). Similarly, references to carbon and oxygen include within their scope respectively ¹²C, ¹³C and ¹⁴C and ¹⁶O and ¹⁸O. The isotopes may be radioactive or non-radioactive. Radiolabelled compounds of Formula I may comprise a radioactive isotope selected from the group of ³H, ¹¹C, ¹⁸F, ¹²¹I, ¹²³I, ¹²⁵I, ¹³¹I, ⁷⁵Br, ⁷⁶Br, ⁷⁷Br and ⁸²Br. Preferably, the radioactive isotope is selected from the group of ³H, ¹¹C and ¹⁸F.

Some compounds of the present invention may exist as atropisomers. Atropisomers are stereoisomers resulting from hindered rotation about single bonds where the steric strain barrier to rotation is high enough to allow for the isolation of the conformers. It is to be understood that all such conformers and mixtures thereof are encompassed within the scope of the present invention.

Where the compounds according to this invention have at least one stereo center, they may accordingly exist as enantiomers or diastereomers. It is to be understood that all such isomers and mixtures thereof are encompassed within the scope of the present invention.

Where the processes for the preparation of the compounds according to the invention give rise to mixture of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography. The compounds may be prepared in racemic form, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution. The compounds may, for example, be resolved into their component enantiomers by standard techniques, such as the formation of diastereomeric pairs by salt formation with an optically active acid, such as (−)-di-p-toluoyl-D-tartaric acid and/or (+)-di-p-toluoyl-L-tartaric acid followed by fractional crystallization and regeneration of the free base. The compounds may also be resolved by formation of diastereomeric esters or amides, followed by chromatographic separation and removal of the chiral auxiliary. Alternatively, the compounds may be resolved using a chiral column vial HPLC or SFC. In some instances rotamers of compounds may exist which are observable by 1H NMR leading to complex multiplets and peak integration in the 1H NMR spectrum.

Chiral centers, of which the absolute configuration is known, are labelled by prefixes R and S, assigned by the standard sequence-rule procedure, and preceded when necessary by the appropriate locants. Chiral centers, of which the relative but not the absolute configuration is known, are labelled arbitrarily by prefixes R* and S*, preceded when necessary by the appropriate locants. These prefixes are assigned by the standard sequence-rule procedure on the arbitrary assumption that the center of chirality with the lowest locant has chirality R. When a compound contains chiral centers with known absolute configurations and a sterically unrelated set of chiral centers with known relative configurations but unknown absolute configurations, then R* and S* are used to designate the latter. (Pure & Appl. Chem. 45, 1976, 11-30). During any of the processes for preparation of the compounds of the present invention, it may be necessary and/or desirable to protect sensitive or reactive groups on any of the molecules concerned. This may be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J. F. W. McOmie, Plenum Press, 1973; and T.W. Greene & P.G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991. The protecting groups may be removed at a convenient subsequent stage using methods known from the art.

Abbreviations

Herein and throughout the application, the following abbreviations may be used.

-   Ac acetyl -   ACN acetonitrile -   BINAP (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene -   Boc tert-butyloxycarbonyl -   br broad -   bu butyl -   Cy cyclohexyl -   d doublet -   dba dibenzylideneacetone -   DBU 1,8-Diazabicyclo(5.4.0)undec-7-ene -   DCE dichloroethane -   DCM dichloromethane -   DIPEA N,N-diisopropylethylamine (Hünig's base) -   DMA N,N-dimethylacetamide -   DMF N,N-dimethylformamide -   DMSO dimethyl sulfoxide -   EDC 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide -   EtOAc ethyl acetate -   ESI electrospray ionization -   Et ethyl -   FCC flash column chromatography -   h hour(s) -   HATU O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium     hexafluorophosphate -   HOBt 1-hydroxybenzotriazole -   HPLC high pressure liquid chromatography -   i-Pr or iPr isopropyl -   Hz Hertz -   LC liquid chromatography -   LAH lithium aluminum hydride -   m multiplet -   M molar (moles/liter) -   Me methyl -   min minute(s) -   MHz megahertz -   μm micrometer -   mm millimeter -   MS mass spectrometry -   N normal -   NBS N-bromosuccinimide -   nm nanometer -   NMR nuclear magnetic resonance -   Piv pivaloyl/pivalic (Me₃CO) -   Pr propyl -   PyBOP (benzotriazol-1-yloxy)tripyrrolidinophosphonium     hexafluorophosphate -   q quartet -   rt room temperature -   s singlet -   SFC supercritical fluid chromatography -   SPhos 2-Dicyclohexylphosphino-2′,6′-dimethoxybiphenyl -   t tertiary -   t triplet -   t-Bu tert-butyl -   TBS tert-butyldimethylsilyl -   TEA triethylamine -   tert tertiary -   TFA trifluoroacetic acid -   THF tetrahydrofuran -   THP tetrahydropyran -   Ts tosyl -   XantPhos 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene -   XtalFluor-E® (Diethylamino)difluorosulfonium tetrafluoroborate

General Schemes:

Compounds of Formula I in the present invention can be synthesized in accordance with the general synthetic methods known to those who are skilled in the art. The following reaction schemes are only meant to represent examples of the invention and are in no way meant to be a limit of the invention.

The compounds of the present invention can be prepared according to Schemes 1-3. Coupling of a 3-pyridyl group to the thiazole ring of compounds of Formula I can be accomplished by coupling the 5-bromopyridine building blocks C-I to the thiazole derivatives B-I in the presence of palladium catalysis, using appropriate ligands, solvents, additives and temperatures to form the 5-(3-pyridyl)-substituted thiazoles A-I (Scheme 1). Alternatively, 5-(3-pyridyl)-substituted thiazoles A-II can be prepared by the coupling of 5-bromopyridine building blocks C-I to thiazole esters B-III in the presence of palladium catalysis, using appropriate ligands, solvents, additives and temperatures. Subsequent ester hydrolysis, using reagents such as potassium tert-butoxide in solvents such as THF, and amide bond formation using reagents such as HATU and DIPEA in solvents such as DMF then provides 5-(3-pyridyl)-substituted thiazoles A-I. Alternatively, direct aminolysis of esters A-II with amines in solvents such as EtOH then affords 5-(3-pyridyl)-substituted thiazoles A-I. When employing hydrochloride salts of amines, direct aminolysis is achieved in suitable solvents such as EtOH in the presence of bases such as DIPEA. In some cases, hydrolysis of esters A-II using reagents such as DIPEA in solvents such as EtOH and water afforded the corresponding carboxylic acids, which were then converted to the corresponding acid chlorides using reagents such as oxallyl chloride and DMF in solvents such as DCM. Amide bond formation could then be achieved using amines in the presence of DIPEA in solvents such as DCM to afford substituted thiazoles A-I.

Preparation of the 2-amino-5-bromopyridines C-I are shown in Scheme 2. 2-Amino-5-bromopyridines C-I can be prepared by direct amination of 5-bromo-2-chloropyridines C-II with amines under microwave conditions. Alternatively, when employing hydrochloride salts of amines, direct amination is achieved in suitable solvents such as acetonitrile in the presence of bases such as DIPEA. Direct amination of 2-bromopyridines C-III with amines under microwave conditions affords intermediates C-IV. Alternatively, intermediates C-IV are prepared by direct amination of 2-chloropyridines C-V with hydrochloride salts of amines in suitable solvents such as acetonitrile in the presence of bases such as DIPEA, or by direct amination of 2-fluoropyridines C-VI with hydrochloride salts of amines in suitable solvents such as DMSO in the presence of bases such as NaHCO₃. In addition, 2-aminopyridines C-IV may be prepared by a palladium mediated amination of 2-bromopyridines C-III or 2-chloropyridines C-V using reagents such as Pd₂(dba)₃. Bromination using reagents such as NBS or bromine affords 2-amino-5-bromopyridines C-I.

The preparation of thiazole derivatives B-I is shown in Scheme 3. B-I can be prepared starting from 2-(alkoxycarbonyl)thiazole-4-carboxylic acid B-II by a process involving standard methods for amide bond formation, ester hydrolysis and a second amide bond formation. Alternatively, intermediates B-III can undergo a direct aminolysis with amines in appropriate solvents and temperatures to afford B-I. Thiazoles B-I can also be prepared by formation of tert-butyl ester B-IV from B-II using tert-butanol and TsCl in the presence of bases such as pyridine. Subsequent selective ester hydrolysis at the 2-position of the thiazole ring and amide bond formation then affords B-V. Alternatively B-V can be formed from B-IV by direct aminolysis with amines in appropriate solvents and temperatures. Subsequent ester hydrolysis using reagents such as TFA followed by amide bond formation then provides B-I.

Intermediates

Compounds of the present invention can be prepared by methods known to those who are skilled in the art. The following examples are only meant to represent examples of the invention and are in no way meant to be a limit of the invention.

Intermediate 1 5-Bromo-N-cyclohexyl-3-(trifluoromethyl)pyridin-2-amine

A solution of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine (250 mg, 0.960 mmol) and cyclohexanamine (571 mg, 5.76 mmol) in a CEM microwave vial was heated in a microwave at 140° C. for 4 h. The reaction mixture was cooled, poured into 1:1 saturated aqueous sodium bicarbonate/water solution and was extracted with ethyl acetate (2×). The combined organic extracts were dried over anhydrous Na₂SO₄, and concentrated to dryness. The residue was redissolved in DCM and purified by FCC (10% EtOAc/hexanes) to give the title compound.

Intermediate 2: Step A N-((1r,3r)-3-Hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 73: Step C, using (1r,3r)-3-aminocyclobutanol in place of methyl 1-(aminomethyl)cyclobutanol.

Intermediate 2: Step B N-((1r,3r)-3-((tert-Butyldimethylsilyl)oxy)cyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

To a solution of N-((1r,3r)-3-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (300 mg, 1.0 mmol, Intermediate 2: Step A), TBSCl (220 mg, 1.5 mmol), and DCM (15 mL) was added imidazole (330 mg, 4.9 mmol) and this mixture was allowed to stir at rt for 16 hours. Water (20 mL) was then added to the reaction followed by extraction with DCM (30 mL×2). The combined organic extracts were dried over anhydrous sodium sulfate and concentrated to dryness. The residue was purified by FCC (0-5% DCM/MeOH) to give the title compound.

Intermediate 3 5-Bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 4 5-Bromo-N-cyclohexyl-3-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-3-(difluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 5 5-Bromo-3-(trifluoromethyl)-N-(3,3,3-trifluoropropyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 3,3,3-trifluoropropan-1-amine in place of cyclohexanamine.

Intermediate 6 5-Bromo-4-(trifluoromethyl)-N-(3,3,3-trifluoropropyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 3,3,3-trifluoropropan-1-amine in place of cyclohexanamine and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 7 5-Bromo-N-cyclobutyl-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using cyclobutanamine in place of cyclohexanamine and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 8 5-Bromo-N-cyclopentyl-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using cyclopentanamine in place of cyclohexanamine and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 9 5-Bromo-2-(cyclohexylamino)nicotinonitrile

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloronicotinonitrile in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 10 5-Bromo-N-cyclohexyl-3-methoxypyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-3-methoxypyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 11 5-Bromo-N-isopropyl-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using isopropylamine in place of cyclohexanamine and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 12 5-Bromo-2-(cyclohexylamino)-4-methylnicotinonitrile

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-4-methylnicotinonitrile in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 13: Step A (S)-tert-Butyl 4,4-difluoro-2-methylpyrrolidine-1-carboxylate

To a solution of triethylamine trihydrofluoride (0.82 mL, 5.0 mmol) and trimethylamine (0.35 mL, 2.5 mmol) in DCM (2 mL) at room temperature in an oven-dried microwave vial were successively added XtalFluor-E® (860 mg, 3.8 mmol) and (S)-1-Boc-2-methylpyrrolidin-4-one (500 mg in 1.9 mL DCE). The reaction was stirred at 80° C. for 90 min then was allowed to cool to room temperature and stirred at room temperature overnight. The reaction was next cooled to 0° C. and slowly quenched with saturated aqueous sodium bicarbonate and was stirred at room temperature for 15 minutes. The reaction was extracted with DCM (3×), dried over anhydrous magnesium sulfate, filtered over Celite®, and concentrated to dryness. The residue was purified by FCC (0-20% EtOAc/hexanes) to give the title compound as a brown oil.

Intermediate 13: Step B (S)-4,4-Difluoro-2-methylpyrrolidine hydrochloride

(S)-tert-Butyl 4,4-difluoro-2-methylpyrrolidine-1-carboxylate (790 mg, 3.6 mmol, Intermediate 13: Step A) was dissolved in HCl (4 M in 1,4-dioxane, 15 mL) and 1,4-dioxane (3.5 mL) at 0° C. and the resulting mixture was allowed to warm to rt and then was stirred at room temperature for 90 minutes. The reaction was concentrated to dryness to give the title compound as a light brown solid.

Intermediate 14 5-Bromo-2-(cyclohexylamino)isonicotinonitrile

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloroisonicotinonitrile in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 15 5-Bromo-N-cyclohexyl-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-4-(difluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 16 5-Bromo-N-cyclohexyl-3-(difluoromethoxy)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-3-(difluoromethoxy)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 17 (R)-5-Bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using (R)-1-cyclopropylethanamine in place of cyclohexanamine and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 18 (S)-5-Bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using (S)-1-cyclopropylethanamine in place of cyclohexanamine and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 19 5-Bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using cyclopentanamine in place of cyclohexanamine and 5-bromo-2-chloro-4-(difluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 20 (S)-5-Bromo-N-(1-cyclopropylethyl)-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using (S)-1-cyclopropylethanamine in place of cyclohexanamine and 5-bromo-2-chloro-4-(difluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 21 (R)-5-Bromo-N-(1-cyclopropylethyl)-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using (R)-1-cyclopropylethanamine in place of cyclohexanamine and 5-bromo-2-chloro-4-(difluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 22 5-Bromo-N-neopentyl-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-4-(trifluoromethyl)pyrimidine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine and neopentylamine in place of cyclohexanamine.

Intermediate 23 5-Bromo-4-(difluoromethyl)-N-neopentylpyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-4-(difluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine and neopentylamine in place of cyclohexanamine.

Intermediate 24 5-Bromo-N-(1-cyclopropylpropyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine and 1-cyclopropylpropan-1-amine in place of cyclohexanamine.

Intermediate 25 5-Bromo-N-(dicyclopropylmethyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine and dicyclopropylmethanamine in place of cyclohexanamine.

Intermediate 26 5-Bromo-N-cyclohexyl-4-methoxypyridin-2-amine

The title compound was prepared as described in Intermediate 1, using 5-bromo-2-chloro-4-(methoxy)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 27 5-Bromo-N-(3,3-difluorocyclohexyl)-3-(trifluoromethyl)pyridin-2-amine

A solution of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine (200 mg, 0.770 mmol), 3,3-difluorocyclohexanamine hydrochloride (395 mg, 2.30 mmol), DIPEA (0.53 mL, 3.1 mmol) and acetonitrile (2.0 mL) were combined in a CEM microwave vial and heated in a microwave at 140° C. for 4 h. The reaction mixture was cooled, poured into 1:1 saturated aqueous sodium bicarbonate/water solution and extracted with ethyl acetate (2×). The combined organic extracts were dried over anhydrous Na₂SO₄, and concentrated to dryness. The residue was purified by FCC (10% EtOAc/hexanes) to give the title compound.

Intermediate 28 5-Bromo-N-(3,3-difluorocyclobutyl)-3-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 27, using 3,3-difluorocyclobutanamine hydrochloride in place of 3,3-difluorocyclohexanamine hydrochloride.

Intermediate 29 5-Bromo-N-(4,4-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 27, using 4,4-difluorocyclohexanamine hydrochloride in place of 3,3-difluorocyclohexanamine hydrochloride and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 30 5-Bromo-N-(3,3-difluorocyclopentyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 27, using 3,3-difluorocyclopentanamine hydrochloride in place of 3,3-difluorocyclohexanamine hydrochloride and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 31 5-Bromo-N-(3,3-difluorocyclobutyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 27, using 3,3-difluorocyclobutanamine hydrochloride in place of 3,3-difluorocyclohexanamine hydrochloride and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 32 5-Bromo-N-(6,6-difluorospiro[3.3]heptan-2-yl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 27, using 6,6-difluorospiro[3.3]heptan-2-amine hydrochloride in place of 3,3-difluorocyclohexanamine hydrochloride and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 33 5-Bromo-N-(3,3-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 27, using 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 34 5-Bromo-N-(spiro[3.3]heptan-2-yl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 27, using spiro[3.3]heptan-2-amine hydrochloride in place of 3,3-difluorocyclohexanamine hydrochloride and 5-bromo-2-chloro-4-(trifluoromethyl)pyridine in place of 5-bromo-2-chloro-3-(trifluoromethyl)pyridine.

Intermediate 35: Step A N-Cyclohexyl-4-methylpyridin-2-amine

A mixture of 2-bromo-4-methylpyridine (500 mg, 2.91 mmol), cyclohexanamine (348 mg, 3.51 mmol), Pd₂(dba)₃ (28 mg, 0.030 mmol), BINAP (91 mg, 0.15 mmol), NaOt-Bu (563 mg, 5.86 mmol) and toluene (20 mL) in a 100 mL round bottom flask was heated to 100° C. for 4 h under a N₂ atmosphere. The crude reaction mixture was concentrated to dryness to give the title compound as a yellow solid which was used in the next step without further purification.

Intermediate 35: Step B 5-Bromo-N-cyclohexyl-4-methylpyridin-2-amine

A mixture of N-cyclohexyl-4-methylpyridin-2-amine (200 mg, 1.05 mmol, Intermediate 35: Step A), NBS (185 mg, 1.04 mmol) and DCM (10 mL) in a round bottom flask was stirred at rt overnight. The mixture was concentrated, the residue was re-dissolved in DCM and purified by FCC (5% EtOAc/petroleum ether) to give the title compound as yellow solid.

Intermediate 36 5-Bromo-N-cyclohexyl-4-cyclopropylpyridin-2-amine

The title compound was prepared as described in Intermediate 35, using 2-bromo-4-cyclopropylpyridine in place of 2-bromo-4-methylpyridine in Step A.

Intermediate 37 5-Bromo-N-cyclohexyl-4-isopropylpyridin-2-amine

The title compound was prepared as described in Intermediate 35, using 2-bromo-4-isopropylpyridine in place of 2-bromo-4-methylpyridine in Step A.

Intermediate 38 5-Bromo-N-cyclohexyl-3-fluoro-4-methylpyridin-2-amine

The title compound was prepared as described in Intermediate 35, using 2-bromo-3-fluoro-4-methylpyridine in place of 2-bromo-4-methylpyridine in Step A.

Intermediate 39: Step A N-Cyclohexyl-4-ethoxypyridin-2-amine

A mixture of 2-chloro-4-ethoxypyridine (200 mg, 1.3 mmol), cyclohexanamine (152 mg, 1.47 mmol), Pd₂(dba)₃ (12 mg, 0.013 mmol), BINAP (40 mg, 0.064 mmol), NaOt-Bu (244 mg, 2.53 mmol) and toluene (5 mL) in a 50 mL round bottom flask fitted with a reflux condenser was heated at 100° C. for 4 h under a N₂ atmosphere. The crude reaction mixture was concentrated to dryness to give the title compound as a red oil that was used in subsequent reactions without further purification.

Intermediate 39: Step B 5-Bromo-N-cyclohexyl-4-ethoxypyridin-2-amine

A mixture of N-cyclohexyl-4-ethoxypyridin-2-amine (154 mg, 0.676 mmol, Intermediate 39: Step A), NBS (123 mg, 0.676 mmol) and DCM (10 mL) in a 50 mL round bottom flask was stirred at rt overnight. The mixture was concentrated to dryness, the residue redissolved in DCM and purified by FCC (5% EtOAc/petroleum ether) to give the title compound as white solid.

Intermediate 40 5-Bromo-N-cyclohexyl-4-ethylpyridin-2-amine

The title compound was prepared as described in Intermediate 39, using 2-chloro-4-ethylpyridine in place of 2-chloro-4-ethoxypyridine in Step A.

Intermediate 41: Step A N-(tert-Butyl)-4-(trifluoromethyl)pyridin-2-amine

To an oven-dried vial under N₂ was added sodium tert-butoxide (1.40 g, 14.6 mmol), BINAP (427 mg, 0.690 mmol), and Pd₂(dba)₃ (312 mg, 0.340 mmol). To this mixture was then added a solution of tert-butylamine (1.00 g, 13.7 mmol) and 2-bromo-4-(trifluoromethyl)pyridine (1.50 g, 6.63 mmol) in THF (15.0 mL, THF was sparged with N₂ for 1 h before use). The vial was then capped and heated to 120° C. for 2 h. The reaction was poured into saturated aqueous sodium bicarbonate and then extracted with ethyl acetate (2×). The combined organic layers were dried over anhydrous sodium sulfate and concentrated to dryness, providing an orange oil that was used in the next step without further purification.

Intermediate 41: Step B 5-Bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine

To a 300 mL round bottom flask under nitrogen was added N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (3.0 g, 14 mmol, Intermediate 41: Step A), NBS (1.9 g, 11 mmol) and DCM (100 mL). The reaction was stirred at rt for 18 h. then poured into saturated aqueous bicarbonate and extracted with ethyl acetate (2×). The combined organic layers were dried (sodium sulfate), filtered and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (10% EtOAc/hexanes) to provide the title compound.

Intermediate 42 5-Bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 1,1,1-trifluoropropan-2-amine in place of tert-butylamine in Step A.

Intermediate 43 (R)-5-Bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using (R)-1,1,1-trifluoropropan-2-amine in place of tert-butylamine in Step A.

Intermediate 44 (S)-5-Bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using (S)-1,1,1-trifluoropropan-2-amine in place of tert-butylamine in Step A.

Intermediate 45 5-Bromo-N-(2-cyclopropylpropan-2-yl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 2-cyclopropylpropan-2-amine in place of tert-butylamine in Step A.

Intermediate 46 5-Bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 1-methylcyclobutanamine hydrochloride in place of tert-butylamine in Step A.

Intermediate 47 5-Bromo-N-(2,2-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 2,2-difluorocyclohexanamine hydrochloride in place of tert-butylamine in Step A.

Intermediate 48 5-Bromo-N-(2-cyclopropylpropan-2-yl)-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 2-cyclopropylpropan-2-amine in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 49 (S)-5-Bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using (S)-1-trifluoromethyl-propylamine in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 50 5-Bromo-4-(difluoromethyl)-N-(tert-pentyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using tert-amylamine in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 51 5-Bromo-N-(tert-pentyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using tert-amylamine in place of tert-butylamine in Step A.

Intermediate 52 5-Bromo-4-(trifluoromethyl)-N-(1-(trifluoromethyl)cyclobutyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 1-(trifluoromethyl)cyclobutan-1-amine in place of tert-butylamine in Step A.

Intermediate 53 (S)-5-Bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using (S)-1-trifluoromethyl-propylamine in place of tert-butylamine in Step A.

Intermediate 54 5-Bromo-4-(trifluoromethyl)-N-((1-(trifluoromethyl)cyclobutyl)methyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using (1-(trifluoromethyl)cyclobutyl)methanamine in place of tert-butylamine in Step A.

Intermediate 55 5-Bromo-N-(3,3,3-trifluoro-2,2-dimethylpropyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 3,3,3-trifluoro-2,2-dimethylpropan-1-amine in place of tert-butylamine in Step A.

Intermediate 56 5-Bromo-4-(difluoromethyl)-N-(1-(trifluoromethyl)cyclobutyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 1-(trifluoromethyl)cyclobutan-1-amine in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 57 5-Bromo-4-(trifluoromethyl)-N-((1-(trifluoromethyl)cyclopropyl)methyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using (1-(trifluoromethyl)cyclopropyl)methanamine in place of tert-butylamine in Step A.

Intermediate 58 5-Bromo-N-(1,1,1-trifluoro-2-methylpropan-2-yl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 1,1,1-trifluoro-2-methylpropan-2-amine in place of tert-butylamine in Step A.

Intermediate 59 5-Bromo-N-(tert-butyl)-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 60 (S)-5-Bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine and (S)-1,1,1-trifluoropropan-2-amine in place of tert-butylamine in Step A.

Intermediate 61: Step A 2-(Cyclohexylamino)-4-(trifluoromethyl)nicotinonitrile

A solution of 2-bromo-4-(trifluoromethyl)nicotinonitrile (250 mg, 0.996 mmol), cyclohexanamine (119 mg, 1.20 mmol), Pd₂(dba)₃ (10 mg, 0.011 mmol), BINAP (32 mg, 0.051 mmol), NaOt-Bu (193 mg, 2.00 mmol), and toluene (5 mL) in a 50 mL round bottom flask fitted with a reflux condenser was heated at 100° C. for 4 h under a N₂ atmosphere. The crude reaction mixture was concentrated to dryness to give the title compound which was used in the next step without purification.

Intermediate 61: Step B 5-Bromo-2-(cyclohexylamino)-4-(trifluoromethyl)nicotinonitrile

A solution of 2-(cyclohexylamino)-4-(trifluoromethyl)nicotinonitrile (100 mg, 0.371 mmol, Intermediate 61: Step A), bromine (1 mL) and acetic acid (12 mL) was stirred at rt overnight in a 50 mL round bottom flask under N₂. The reaction mixture was poured into a solution of saturated aqueous Na₂S₂O₃ (10 mL), extracted with ethyl acetate (2×20 mL), dried over anhydrous MgSO₄, and concentrated to dryness. The residue was purified by FCC (5% EtOAc/petroleum ether) to give the title compound.

Intermediate 62: Step A Ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

5-Bromo-N-cyclopentyl-4-(difluoromethyl) pyridin-2-amine (870 mg, 3.0 mmol, Intermediate 19), (S)-ethyl 4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (720 mg, 2.7 mmol, Intermediate 73, Step A), Pd(OAc)₂ (67 mg, 0.30 mmol), PCy₃.HBF₄ (220 mg, 0.60 mmol), pivalic acid (122 mg, 1.20 mmol), K₂CO₃ (1.66 g, 12.0 mmol), and DMA (10 mL) were added to a 20 mL microwave tube under Ar. The resultant mixture was sparged with Ar for 5 minutes and then stirred at 120° C. in the microwave for 1 hour. The crude reaction was cooled to room temperature and concentrated to dryness to give the crude product. Purification by FCC (10-50% petroleum ether/EtOAc) then afforded the title compound as a white solid.

Intermediate 62: Step B Potassium(S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylicacid

t-BuOK (140 mg, 1.2 mmol) was added to a mixture consisting of (S)-ethyl 5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (540 mg, 1.1 mmol, Intermediate 62: Step A), H₂O (0.5 mL), and THF (2 mL) in a 25 mL round bottom flask. The resultant mixture was stirred at 60° C. for 2 hours before diluting with H₂O (20 mL) and extracting with dichloromethane (20 mL×2). The aqueous layer was frozen using dry ice/acetone and then lyophilized to dryness to afford the title compound as a white solid.

Intermediate 63: Step A 4-(Trifluoromethyl)-N-(1-(trifluoromethyl)cyclopropyl)pyridin-2-amine

To an oven-dried vial under N₂ was added sodium tert-butoxide (357 mg, 3.70 mmol), BINAP (111 mg, 0.180 mmol) and Pd₂(dba)₃ (81 mg, 0.088 mmol). Then, a solution of 1-(trifluoromethyl)cyclopropanamine (464 mg, 3.60 mmol) and 2-bromo-4-(trifluoromethyl)pyridine (400 mg, 1.77 mmol) in THF (3.9 mL) was added and the resulting mixture was stirred at rt for 3.5 hours. The mixture was partitioned between saturated aqueous NaHCO₃ (30 mL) and EtOAc (30 mL), and the aqueous layer was further extracted with EtOAc (2×25 mL). The organic layers were combined, dried over anhydrous Na₂SO₄, filtered and concentrated to dryness to provide the title compound as a yellow-orange oil, which was used without further purification.

Intermediate 63: Step B 5-Bromo-4-(trifluoromethyl)-N-(1-(trifluoromethyl)cyclopropyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41: Step B, using 4-(trifluoromethyl)-N-(1-(trifluoromethyl)cyclopropyl)pyridin-2-amine (Intermediate 63: Step A) in place of N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine.

Intermediate 64: Step A N-(2,2-Difluorocyclopentyl)-4-(trifluoromethyl)pyridin-2-amine

To an oven-dried vial under N₂ was added 2,2-difluorocyclopentan-1-amine.HCl (400 mg, 2.40 mmol) and NaHCO₃ (213 mg, 2.50 mmol). Then a mixture of 2-fluoro-4-(trifluoromethyl)pyridine (203 mg, 1.20 mmol) in DMSO (2 mL, sparged with nitrogen for 1 hour prior to addition) was added and the resulting mixture was stirred at 140° C. for 20 hours. The mixture was cooled to rt and partitioned between saturated aqueous NaHCO₃ (20 mL) and EtOAc (20 mL). The layers were separated and the aqueous layer further extracted with EtOAc (20 mL). The organic layers were combined, washed with water (2×15 mL), dried over anhydrous Na₂SO₄, filtered and concentrated to dryness to provide the title compound as a brown oil, which was taken on without further purification.

Intermediate 64: Step B 5-Bromo-N-(2,2-difluorocyclopentyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41: Step B, using N-(2,2-difluorocyclopentyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 64: Step A) in place of N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine.

Intermediate 65: Step A 2-(Ethoxycarbonyl)thiazole-4-carboxylicacid

To a 3-neck, 200 mL round bottom flask under nitrogen was added 3-bromo-2-oxopropanoic acid (5 g, 30 mmol) and anhydrous 1,4-dioxane (50 mL). To this mixture was added ethyl 2-amino-2-thioxoacetate (4.1 g, 31 mmol) and the mixture heated at 50° C. for 1.5 h. The reaction was concentrated to dryness, the residue was dissolved in saturated aqueous NaHCO₃ (100 mL) and water (100 mL), and the aqueous solution extracted with ethyl acetate (4×100 mL). The aqueous layer was acidified to pH ˜2 with concentrated HCl. After precipitate formation (˜20 min) the aqueous mixture was extracted with ethyl acetate (3×100 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated to dryness to give the title compound as a red solid, which was used in next step without further purification.

Intermediate 65: Step B Ethyl 4-(4-fluoropiperidine-1-carbonyl)thiazole-2-carboxylate

To a 200 mL round bottom flask under N₂ was added 2-(ethoxycarbonyl)thiazole-4-carboxylic acid (2.5 g, 12 mmol, Intermediate 65: Step A) and DMF (65 mL). Once the acid was in solution, PyBOP (9.7 g, 19 mmol) and methylmorpholine (2.9 g, 29 mmol) were added. After 10 min. 4-fluoropiperidine (2.3 g, 16 mmol) was added and the reaction was allowed to stir overnight at rt. The reaction was then diluted with ethyl acetate, washed with saturated aqueous sodium bicarbonate (1×), water (2×), and brine (1×), dried over anhydrous Na₂SO₄, filtered and concentrated to dryness. The residue was dissolved in DCM and purified by FCC (0-80% EtOAc/hexanes) to give the title compound.

Intermediate 65: Step C 4-(4-Fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

To a 100-mL round bottom flask was added ethyl 4-(4-fluoropiperidine-1-carbonyl)thiazole-2-carboxylate (0.76 g, 2.6 mmol, Intermediate 65: Step B) and toluene (13 mL). A solution of 1-amino-2-methylpropan-2-ol (473 mg, 5.31 mmol) in toluene (5 mL) was then added to the reaction mixture, followed by K₂CO₃ (0.73 g, 5.3 mmol). The reaction was heated to 90° C. and allowed to stir at that temperature for 18 h. The reaction was cooled, diluted with water, and extracted with ethyl acetate (3×). The combined organic layers were washed with water, followed by brine, then dried over anhydrous Na₂SO₄ and concentrated to dryness. The residue was dissolved in DCM and purified by FCC (0-80% EtOAc/hexanes) to give the title compound.

Intermediate 66: Step A 4-tert-Butyl 2-ethyl thiazole-2,4-dicarboxylate

A round bottom flask under N₂ containing 2-(ethoxycarbonyl)thiazole-4-carboxylic acid (2.0 g, 9.9 mmol, Intermediate 65: Step A), tert-BuOH (18 mL, 190 mmol), and pyridine (5 mL) was cooled to 0° C. in an ice bath, and then TsCl (4.4 g, 23 mmol) was added in one portion. The reaction was allowed to warm to rt gradually over 1 h and stirred for 18 h. The reaction was quenched by the addition of saturated aqueous potassium carbonate (100 mL) and water (100 mL) and the mixture stirred for 30 min. The mixture was then extracted with ether (3×100 mL) and the combined organic layers were washed with 5% saturated aqueous K₂CO₃ (2×100 mL) and 5% saturated aqueous K₂CO₃ in brine (1×100 mL). The combined organic layers were then dried over anhydrous Na₂SO₄, and concentrated to dryness. The residue was purified by FCC (0-80% EtOAc/hexanes) to give the title compound.

Intermediate 66: Step B tert-Butyl 2-((2-hydroxy-2-methylpropyl)carbamoyl)thiazole-4-carboxylate

The title compound was prepared as described in Example 65, Step C, using 4-tert-butyl 2-ethyl thiazole-2,4-dicarboxylate (Intermediate 66: Step A) in place of ethyl 4-(4-fluoropiperidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 66: Step C 2-((2-Hydroxy-2-methylpropyl)carbamoyl)thiazole-4-carboxylic acid

A solution of tert-butyl 2-((2-hydroxy-2-methylpropyl)carbamoyl)thiazole-4-carboxylate (1.0 g, 3.3 mmol, Intermediate 66: Step B) in 1:1 TFA:DCM (20 mL) was allowed to stand for 1 h. The reaction was concentrated to dryness and the residue was placed under high vacuum overnight to give the title compound, which was used in next step without purification.

Intermediate 66: Step D (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

To a 100 mL round bottom flask under nitrogen containing 2-((2-hydroxy-2-methylpropyl)carbamoyl)thiazole-4-carboxylic acid (806 mg, 3.30 mmol, Intermediate 66: Step C) was added, DMF (20 mL) followed by PyBOP (2.6 g, 5.0 mmol) and methylmorpholine (1.10 g, 10.9 mmol). After 10 min. (S)-2-methylpiperidine (491 mg, 4.90 mmol) was added and the reaction allowed to stir overnight at rt. The reaction was poured into ethyl acetate and washed with water (3×) and brine (1×). The organic layer was dried over anhydrous sodium sulfate and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-50% EtOAc/hexanes) to provide the title compound.

Intermediate 67 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 66: Step D, using (S)-4,4-difluoro-2-methylpyrrolidine hydrochloride (Intermediate 13: Step B) in place of (S)-2-methylpiperidine.

Intermediate 68 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylazetidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 66: Step D, using (S)-2-methylazetidine hydrochloride in place of (S)-2-methylpiperidine.

Intermediate 69 (S)—N-2-Hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 66: Step D, using (S)-2-methylpyrrolidine in place of (S)-2-methylpiperidine.

Intermediate 70: Step A Ethyl-4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate

In a 200 mL round bottom flask under N₂ was added 2-(ethoxycarbonyl)thiazole-4-carboxylic acid (6.0 g, 30 mmol, Intermediate 65, Step A) and methyl THP (70 mL). This mixture was cooled to 0° C. then (1s,4s)-7-azabicyclo[2.2.1]heptane was added (4.4 g, 33 mmol). Propyl phosphonic anhydride solution (>50% by wt. % in EtOAc) was then added (28 mL, 44 mmol) followed by addition of DIPEA (16 mL, 95 mmol). The mixture was allowed to warm to rt and stirred at rt for 18 h. The reaction was then poured into saturated aqueous sodium bicarbonate and extracted with ethyl acetate (4×). The combined organic layers were washed with brine (1×), dried over anhydrous sodium sulfate and concentrated to dryness to provide the title compound, which was used in next step without further purification.

Intermediate 70: Step B 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

In a 2-neck 200 mL flask under N₂ was added ethyl-4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (9.5 g, 34 mmol, Intermediate 70, Step A), 1-amino-2-methylpropan-2-ol (13.3 g, 149 mmol) and EtOH (100 mL), and the reaction was stirred at rt for 18 h. The reaction mixture was then poured into saturated aqueous sodium bicarbonate and extracted with EtOAc (5×). The combined organic layers were washed with brine (1×), dried over anhydrous sodium sulfate and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-10% DCM/MeOH) to provide the title compound.

Intermediate 71 4-(4,4-Difluoropiperidine-1-carbonyl)-N-(3-hydroxy-3-methylbutyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 70, using 4,4-difluoropiperidine in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in step A and 4-amino-2-methylbutan-2-ol in place of 1-amino-2-methylpropan-2-ol in step B.

Intermediate 72: Step A 4-(tert-Butoxycarbonyl)thiazole-2-carboxylic acid

To a solution of 4-tert-butyl 2-ethyl thiazole-2,4-dicarboxylate (5.0 g, 19 mmol, Intermediate 66: Step A) in THF (50 mL) was added aqueous LiGH (21 mL, 1 M, 21 mmol) drop-wise over 2 min at rt and the resulting mixture was stirred at rt for 5 h. The reaction was concentrated to dryness and the residue was acidified with aqueous 1 M HCl to pH 6 and lyophilized to give the title compound as a white solid, which was used in the next step without further purification.

Intermediate 72: Step B tert-Butyl 2-((1,1-dioxidotetrahydro-2H-thiopyran-4-yl)carbamoyl)thiazole-4-carboxylate

To a 250-mL round bottom flask under N₂ was added 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid (6.0 g, 20 mmol, Intermediate 72: Step A), 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride (4.4 g, 24 mmol), HATU (9.0 g, 24 mmol), DIPEA (7.7 g, 60 mmol) and DMF (30 mL). This mixture was allowed to stir at rt for 16 h followed by dilution with water (50 mL) and extraction with EtOAc (50 mL×3). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried over anhydrous sodium sulfate, filtered, and concentrated to dryness. The residue was recrystallized from EtOAc (50 mL) to give the title compound as a white solid.

Intermediate 72: Step C 2-((1,1-Dioxidotetrahydro-2H-thiopyran-4-yl)carbamoyl)thiazole-4-carboxylic acid

tert-Butyl 2-((1,1-dioxidotetrahydro-2H-thiopyran-4-yl)carbamoyl)thiazole-4-carboxylate (1.0 g, 2.8 mmol, Intermediate 72: Step B) was dissolved in 1:1 TFA:DCM (20 mL) and allowed to stand for 1 h. The reaction was concentrated to dryness and the residue placed on high vacuum overnight to give the title compound, which was used in the next step without purification.

Intermediate 72: Step D (S)—N-(1,1-Dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

To a 100 mL round bottom flask, under N₂, containing 2-((1,1-dioxidotetrahydro-2H-thiopyran-4-yl)carbamoyl)thiazole-4-carboxylic acid (500 mg, 1.6 mmol, Intermediate 72: Step C) was added DMF (10 mL) followed by PyBOP (1.3 g, 2.5 mmol) and methylmorpholine (0.55 g, 5.4 mmol). After 10 min (S)-2-methylpiperidine (244 mg, 2.52 mmol) in DMF (5.0 mL) was added and the reaction was allowed to stir overnight at 50° C. The reaction was then poured into ethyl acetate and washed with water (3×) and brine (1×). The organic layer was dried over anhydrous sodium sulfate and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-50% ethyl acetate/hexanes) to provide the title compound.

Intermediate 73: Step A Ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 65: Step B, using (S)-2-methylpyrrolidine in place of 4-fluoropiperidine

Intermediate 73: Step B Potassium (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

A solution of (S)-ethyl 4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (7.5 g, 28 mmol, Intermediate 73: Step A), potassium t-butoxide (3.44 g, 311 mmol), THF (160 mL), and H₂O (4 mL) was stirred at 60° C. for 2 hours. The reaction was diluted with H₂O (30 mL) and extracted with DCM (30 mL×2). The aqueous layer was collected and lyophilized to dryness to give the title compound as a yellow solid.

Intermediate 73: Step C (S)—N-((1-Hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

To a 300 mL round bottom flask under N₂ was added EDC.HCl (4.9 g, 26 mmol), 1-(aminomethyl)cyclobutanol (1.3 g, 13 mmol), potassium (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (3.6 g, 13 mmol, Intermediate 73: Step B), HOBt (3.5 g, 26 mmol), DIPEA (6.8 mL, 39 mmol) and THF (100 mL). The resultant mixture was stirred at room temperature for 16 hours before diluting with ethyl acetate (200 mL). This mixture was washed with H₂O (50 mL) and brine (30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated to dryness to give the crude product, which was purified by preparative HPLC. The purified material was suspended in water (10 mL), the mixture frozen using dry ice/acetone, and then lyophilized to dryness to afford the title compound as a white solid.

Intermediate 74 4-((S)-2-Methylpyrrolidine-1-carbonyl)-N-((1r,3r)-3-(methylsulfonyl)cyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 73: Step C substituting (1r,3r)-3-(methylsulfonyl)cyclobutanamine in place of 1-(aminomethyl)cyclobutanol.

Intermediate 75 (S)—N-((3-Hydroxyoxetan-3-yl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 73: Step C substituting 3-(aminomethyl)oxetan-3-ol in place of 1-(aminomethyl)cyclobutanol.

The following intermediates can be prepared by procedures described.

Intermediate 76: Step A 2-Methyl-2-((trimethylsilyl)oxy)propanenitrile

To a flask containing acetone (2 mL, 27.1 mmol), zinc iodide (173 mg, 0.54 mmol) and DCM (55 mL) is added trimethylsilyl cyanide (4.4 mL, 35.2 mmol), and the resulting mixture stirred at rt for 18 hours. The mixture is diluted with saturated aqueous NaHCO₃, the layers separated, and the aqueous layer further extracted with DCM. The organics are combined, dried over MgSO₄, filtered and concentrated to dryness to give the title compound.

Intermediate 76: Step B tert-Butyl (2-hydroxy-2-methylpropyl-1,1-d₂)carbamate

To a sealed tube containing borane-d₃ (7 mL, 7 mmol, 1 M in THF) is added 2-methyl-2-((trimethylsilyl)oxy)propanenitrile (1.3 g, 7 mmol, Intermediate 76: Step A) and the resulting solution is stirred at 65° C. for 15 hours. The mixture is allowed to cool to rt, then water is added until the evolution of H₂ ceases. The mixture is then warmed to 60° C. and the THF is removed under a stream of N₂. The solution is allowed to cool to rt, then aqueous 1 N HCl (3 mL) is added followed by concentrated HCl (1 mL) slowly. The resulting mixture is stirred at 60° C. for 6 hours, then cooled to rt, diluted with THF (8 mL) and neutralized with 10 M aqueous NaOH. Then, Boc-anhydride (1.5 mL, 7 mmol) is added and the reaction is stirred at rt for 15 hours. The mixture is diluted with EtOAc, the layers separated, and the aqueous layer further extracted with EtOAc. The combined organic layers are dried over anhydrous MgSO₄ and concentrated to dryness to provide the crude product. The crude material is purified by FCC (0-60% EtOAc/hexanes) to provide the title compound.

Intermediate 76: Step C 1-Amino-2-methylpropan-1,1-d₂-2-olhydrochloride

A mixture of tert-butyl (2-hydroxy-2-methylpropyl-1,1-d₂)carbamate (1.2 g, 6.4 mmol, Intermediate 76: Step B), TFA (5.9 mL, 76 mmol) and DCM (22 mL) is stirred at rt for 15 hours.

The solution is concentrated to dryness then dissolved in DCM/MeOH. HCl (1.8 mL, 7.0 mmol, 4 M in 1,4-dioxane) is then added and the resulting solution is concentrated to dryness. The residue is suspended in EtOAc/hexane and stirred vigorously under a stream of N₂. The mixture is filtered and the solids rinsed with hexane. The solids are then dissolved in MeOH and concentrated to dryness to afford the title compound.

Intermediate 76: Step D (S)—N-(2-Hydroxy-2-methylpropyl-1,1-d₂)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound is prepared as described in Intermediate 70 using (S)-2-methylpyrrolidine in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and 1-amino-2-methylpropan-1,1-d₂-2-ol hydrochloride (Intermediate 76: Step C) in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 77: Step A 2-(Methyl-d₃)-2-((trimethylsilyl)oxy)propanenitrile-3,3,3-d₃

The title compound is prepared as described in Intermediate 76: Step A using acetone-d₆ in place of acetone.

Intermediate 77: Step B 2-(Aminomethyl)propan-1,1,1,3,3,3-d₆-2-olhydrochloride

2-(Methyl-d₃)-2-((trimethylsilyl)oxy)propanenitrile-3,3,3-d₃ (11.64 g, 71.3 mmol, Intermediate 77: Step A) is added to a suspension of LAH (5.4 g, 142.5 mmol, 1 M in THF) in THF (150 mL) at 0-5° C. The resulting suspension is allowed to warm to rt overnight. The solution is then cooled to 0° C. and water (5.4 mL), 15% aqueous NaOH (5.4 mL) and water (16 mL) are added sequentially dropwise. The mixture is allowed to warm to rt over 20 minutes and then is filtered through Celite® and the filter cake washed with THF. The filtrate and wash are combined and concentrated to dryness. The residue is diluted with THF and then HCl (12.5 mL, 50 mmol, 4 M in 1,4-dioxane) is added and the resulting mixture is concentrated to dryness. EtOAc is added to the residue and the product solidified. The solids are collected by filtration, washed with EtOAc, dissolved in MeOH and concentrated to dryness to provide the title compound.

Intermediate 77: Step C (S)—N-(2-Hydroxy-2-(methyl-d₃)propyl-3,3,3-d₃)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound is prepared as described in Intermediate 70 using (S)-2-methylpyrrolidine in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and 2-(aminomethyl)propan-1,1,1,3,3,3-d₆-2-ol hydrochloride (Intermediate 77: Step B) in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 78 (S)—N-((1-Hydroxycyclopropyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound can be prepared as described in Intermediate 70 using (S)-2-methylpyrrolidine in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and 1-(aminomethyl)cyclopropan-1-ol in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 79 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(3-hydroxy-3-methylcyclobutyl)thiazole-2-carboxamide

The title compound can be prepared as described in Intermediate 70 using (S)-4,4-difluoro-2-methylpyrrolidine hydrochloride (Intermediate 13: Step B) in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and 3-amino-1-methylcyclobutan-1-ol in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 80 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(1,1-dioxidothietan-3-yl)thiazole-2-carboxamide

The title compound can be prepared as described in Intermediate 70 using (S)-4,4-difluoro-2-methylpyrrolidine hydrochloride (Intermediate 13: Step B) in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and 3-aminothietane 1,1-dioxide in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 81 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(1-hydroxy-2-methylpropan-2-yl)thiazole-2-carboxamide

The title compound can be prepared as described in Intermediate 70 using (S)-4,4-difluoro-2-methylpyrrolidine hydrochloride (Intermediate 13: Step B) in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and 2-amino-2-methylpropan-1-ol in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 82 (4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)thiazol-2-yl)(3-hydroxy-3-methylazetidin-1-yl)methanone

The title compound can be prepared as described in Intermediate 70 using 3-methylazetidin-3-ol in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 83 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(1-hydroxy-2-methylpropan-2-yl)-N-methylthiazole-2-carboxamide

The title compound can be prepared as described in Intermediate 70 using 2-methyl-2-(methylamino)propan-1-ol in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 84 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-N-methylthiazole-2-carboxamide

The title compound can be prepared as described in Intermediate 70 using 2-methyl-1-(methylamino)propan-2-ol in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 85 N-(3-Hydroxy-3-methylbutan-2-yl)-N-methyl-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound can be prepared as described in Intermediate 70 using (S)-2-methylpiperidine in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and 2-methyl-3-(methylamino)butan-2-ol in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 86 (S)-4-(2-Methylpiperidine-1-carbonyl)-N-(oxetan-3-yl)thiazole-2-carboxamide

The title compound can be prepared as described in Intermediate 70 using (S)-2-methylpiperidine in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and oxetan-3-amine in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 87 (S)-(2-(2,2-Dioxido-2-thia-6-azaspiro[3.3]heptane-6-carbonyl)thiazol-4-yl)(2-methylpiperidin-1-yl)methanone

The title compound can be prepared as described in Intermediate 70 using (S)-2-methylpiperidine in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and 2-thia-6-azaspiro[3.3]heptane 2,2-dioxide in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 88 (S)-(2-(1,1-Dioxidothiomorpholine-4-carbonyl)thiazol-4-yl)(2-methylpiperidin-1-yl)methanone

The title compound can be prepared as described in Intermediate 70 using (S)-2-methylpiperidine in place of (1s,4s)-7-azabicyclo[2.2.1]heptane in Step A and thiomorpholine 1,1-dioxide in place of 1-amino-2-methylpropan-2-ol in Step B.

Intermediate 89 5-Bromo-N-(1-cyclobutylethyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 1-cyclobutylethan-1-amine in place of tert-butylamine in Step A.

Intermediate 90 5-Bromo-N-(1-cyclopropylpropyl)-4-difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 1-cyclopropylpropan-1-amine in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 91 5-Bromo-N-(1-methylcyclobutyl)-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using 1-methylcyclobutanamine hydrochloride in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 92 5-Bromo-N-(dicyclopropylmethyl)-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using dicyclopropylmethanamine in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 93 Ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

To a 300 mL screw cap pressure vessel under N₂ was added 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine (6.5 g, 21.0 mmol, Intermediate 46), ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (4.3 g, 14.1 mmol, Intermediate 109: Step A), potassium carbonate (3.9 g, 28.2 mmol) and DMF (150 mL, purged with N₂ for 1 h). To this mixture was added bis(tri-t-butylphosphine)Pd (0), (1.4 g, 2.7 mmol) and the reaction capped and heated to 130° C. for 8 h. The reaction was then cooled to rt and poured into saturated aqueous bicarbonate. The aqueous layer was extracted with ethyl acetate (3×), then the combined organic layers were dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude residue was re-dissolved in DCM and purified by FCC (0-80% ethyl acetate/hexanes) to afford a tan colored foamy solid after removal of the solvent under reduced pressure.

Intermediate 94 Ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 95 Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting 5-bromo-N-(1-methylcyclobutyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 91) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 96 Ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine.

Intermediate 97 Ethyl 5-(6-(((S)-1-cyclopropylethyl)amino)-4-(difluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 20) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine.

Intermediate 98 Ethyl 5-(6-(((S)-1-cyclopropylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 18) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine.

Intermediate 99 Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 100 Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 53) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 101: Step A (E/Z)-2-(2-((tert-Butyldimethylsilyl)oxy)vinyl)isoindoline-1,3-dione

To a 250 mL round-bottom flask was added N-(2-oxoethyl)phthalimide (6 g, 31.7 mmol), tert-butyldimethylsilyl trifluoromethanesulfonate (8.7 mL, 37.9 mmol) and DCM (100 mL). Then DBU (5.4 mL, 36.1 mmol) was added dropwise and the resulting yellow solution was stirred at rt for 1 hour. The solution was washed with 1 M aqueous H₂SO₄ (50 mL) and the aqueous layer was extracted with DCM (2×50 mL). The organic layers were combined, washed with water (50 mL), saturated aqueous NaHCO₃ (50 mL) and dried over anhydrous sodium sulfate. The mixture was filtered and concentrated to dryness. The crude residue was purified by FCC (0-5% EtOAc/Hexanes) to provide the title compounds as yellow oils.

Intermediate 101: Step B1 2-((1S*,2R*)-2-((tert-Butyldimethylsilyl)oxy)cyclopropyl)isoindoline-1,3-dione

To an oven-dried 500 mL round-bottom flask was added (Z)-2-(2-((tert-butyldimethylsilyl)oxy)vinyl)isoindoline-1,3-dione (4.28 g, 14.11 mmol, Intermediate 101: Step A) and dry benzene (71 mL) and the resulting solution was cooled to 0° C. in an ice-bath. Then, Et₂Zn (212 mL, 212 mmol, 1 M in hexanes) was added followed by CH₂I₂ (17 mL, 212 mmol) and the mixture was allowed to slowly warm to rt and then stirred at rt for 21 hours. The mixture was partitioned between 1 N aqueous H₂SO₄ (100 mL) and hexanes (100 mL). The layers were separated and the organic layer was washed with water (100 mL) followed by saturated aqueous NaHCO₃ (100 mL) and then dried over anhydrous sodium sulfate. The mixture was filtered and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-10% EtOAc/Hexanes) to provide the title compound.

Intermediate 101: Step B2 2-((1R*,2R*)-2-((tert-Butyldimethylsilyl)oxy)cyclopropyl)isoindoline-1,3-dione

To an oven-dried 500 mL round-bottom flask was added (Z)-2-(2-((tert-butyldimethylsilyl)oxy)vinyl)isoindoline-1,3-dione (4.28 g, 14.11 mmol, Intermediate 101: Step A) and dry benzene (71 mL) and the resulting solution was cooled to 0° C. in an ice-bath. Then, Et₂Zn (212 mL, 212 mmol, 1 M in hexanes) was added followed by CH₂I₂ (17 mL, 212 mmol) and the mixture was allowed to slowly warm to rt and then stirred at rt for 21 hours. The mixture was partitioned between 1 N aqueous H₂SO₄ (100 mL) and hexanes (100 mL). The layers were separated and the organic layer was washed with water (100 mL) followed by saturated aqueous NaHCO₃ (100 mL) and then dried over anhydrous sodium sulfate. The mixture was filtered and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-10% EtOAc/Hexanes) to provide the title compound.

Intermediate 101: Step C trans-(1R*,2R*)-2-((tert-Butyldimethylsilyl)oxy)cyclopropan-1-amine

To a 200 mL round-bottom flask was added 2-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)isoindoline-1,3-dione (4.53 g, 14.27 mmol, Intermediate 101: Step B2), DCM (55 mL) and EtOH (11 mL). Then, hydrazine hydrate (4.16 mL, 85.62 mmol) was added and the resulting solution was stirred at rt for 4 hours. The mixture was filtered through a pad of Celite® and the solution concentrated to dryness. The crude material was dissolved in DCM and washed with saturated aqueous NaHCO₃. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to dryness to provide the title compound as a yellow oil.

Intermediate 101: Step D N-((1R*,2R*)-2-((tert-Butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting trans-(1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropan-1-amine (Intermediate 101: Step C) for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 101: Step E cis-(1S*,2R*)-2-((tert-Butyldimethylsilyl)oxy)cyclopropan-1-amine

The title compound was prepared as described for Intermediate 101: Step C substituting 2-((1S*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)isoindoline-1,3-dione (Intermediate 101: Step B1) for 2-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)isoindoline-1,3-dione.

Intermediate 101: Step F1 N-((1R*,2*S)-2-((tert-Butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting cis-(1*S,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropan-1-amine (Intermediate 101: Step E) for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Whelk O1 (S,S), 5 μm, 250×21.1 mm, Mobile phase: 22% iPrOH+0.3% iPrNH₂, 78% CO₂, first eluting enantiomer).

Intermediate 101: Step F2 N-((1S*,2R*)-2-((tert-Butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting cis-(1S*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropan-1-amine (Intermediate 101: Step E) for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Whelk O1 (S,S), 5 μm, 250×21.1 mm, Mobile phase: 22% iPrOH+0.3% iPrNH₂, 78% CO₂, second eluting enantiomer).

Intermediate 101: Step G1 N-((1R*,2R*)-2-((tert-Butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 101: Step D substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 7.5% iPrOH+0.3% iPrNH₂, 92.5% CO₂, first eluting enantiomer).

Intermediate 101: Step G2 N-((1S*,2S*)-2-((tert-Butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 101: Step D substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 7.5% iPrOH+0.3% iPrNH₂, 92.5% CO₂, second eluting enantiomer).

Intermediate 102 Ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 103 Ethyl 4-((S)-2-methylpyrrolidine-1-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 53) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 104: Step A (R)-5-Bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using (R)-1,1,1-trifluoro-2-butylamine in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 104: Step B Ethyl 5-(4-(difluoromethyl)-6-(((R)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting (R)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 104: Step A) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 105 trans-N-((1R*,2R*)-2-((tert-Butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting trans-(1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropan-1-amine (Intermediate 101: Step C) for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 106 Ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 59) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 107 Ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 41: Step B) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 108: Step A Ethyl(S)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 70: Step A, using (S)-2-methylpiperidine in place of (s,4s)-7-azabicyclo[2.2.1]heptane.

Intermediate 108: Step B Ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl(S)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 108: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 109: Step A Ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 70: Step A, using (S)-4,4-difluoro-2-methylpyrrolidine hydrochloride (Intermediate 13: Step B) in place of (1s,4s)-7-azabicyclo[2.2.1]heptane.

Intermediate 109: Step B Ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 109: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 110 Ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 59) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 109: Step A) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 111 2-(Aminomethyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

To a 25 mL round-bottom flask was added ammonium hydroxide solution (2.8 mL, 21.6 mmol, 30% in H₂O) and Et₂O (2.77 mL). Then, 2,2-bis(trifluoromethyl)oxirane (1 mL, 8.3 mmol) was added slowly and the resulting mixture stirred at rt for 3.5 hours. Et₂O (10 mL) was added and the layers were separated. The aqueous layer was extracted further with Et₂O (15 mL) and then the organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated to dryness at low temperature to provide the title compound as a white solid.

Intermediate 112 5-Bromo-4-(difluoromethyl)-N-((1-(trifluoromethyl)cyclobutyl)methyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using [1-(trifluoromethyl)cyclobutyl]methanamine in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 113 5-Bromo-4-(difluoromethyl)-N-((1-(trifluoromethyl)cyclopropyl)methyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using [1-(trifluoromethyl)cyclopropyl]methanamine HCl in place of tert-butylamine and 2-bromo-4-(difluoromethyl)pyridine in place of 2-bromo-4-(trifluoromethyl)pyridine in Step A.

Intermediate 114 5-Bromo-N-((1-methylcyclopropyl)methyl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using (1-methylcyclopropyl)methanamine HCl in place of tert-butylamine in Step A.

Intermediate 115 (R)-5-Bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 41, using (R)-1-trifluoromethyl-propylamine in place of tert-butylamine in Step A.

Intermediate 116 Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 117 Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate

Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (1.0 g, 3.6 mmol, Intermediate 70: Step A), (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (1.25 g, 3.92 mmol, Intermediate 60), pivalic acid (146 mg, 1.43 mmol), K₂CO₃ (1.97 g, 14.3 mmol), 4 Å molecular sieves (2.0 g), and DMA (25 mL) were added to a 50 mL round-bottomed flask. The mixture was sparged with N₂ for 5 minutes and then treated with Pd(OAc)₂ (80 mg, 0.36 mmol), PCy₃.HBF₄ (260 mg, 0.707 mmol). The resultant mixture was sparged with N₂ for another 5 minutes and then stirred at 95° C. for 16 hours before cooling to room-temperature, quenching with water (50 mL), and extracting with ethyl acetate (50 mL×2). The combined organic extracts were dried over anhydrous Na₂SO₄, filtered, and concentrated to dryness under reduced pressure to afford the crude product, which was purified by preparative HPLC. The product was lyophilized from water to afford the title compound as a white solid.

Intermediate 118: Step A N-(1-Cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine

2-Bromo-4-(difluoromethyl)pyridine (500 mg, 2.40 mmol), and (S)-1-cyclopropyl-2,2,2-trifluoroethanamine (633 mg, 3.61 mmol), t-BuONa (693 mg, 7.22 mmol) were dissolved t-amyl-OH (10 mL). The resultant mixture was sparged with Ar for 5 min and then treated with SPhos-Pd-G3.DCM (103 mg, 0.119 mmol). The mixture was sparged with Ar for another 5 min and then stirred at 95° C. for 15 hours before quenching with water (20 mL) and extracting with ethyl acetate (30 mL×2). The combined organic extracts were dried over anhydrous Na₂SO₄, filtered, and concentrated to dryness under reduced pressure to give the crude product, which was purified by FCC (0-20% ethyl acetate/petroleum ether) to afford the title compound as a yellow oil.

Intermediate 118: Step B 5-Bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine

NBS (235 mg, 1.32 mmol) was added in portions to a solution consisting of N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (440 mg, 1.65 mmol, Intermediate 118: Step A) and MeCN (30 mL). The resultant mixture was stirred at room temperature for 2 hours before quenching with water (20 mL) and extracting with ethyl acetate (50 mL×2). The combined organic extracts were dried over anhydrous Na₂SO₄, filtered, and concentrated to dryness under reduced pressure to give the crude product, which was purified by FCC (0-10% ethyl acetate/petroleum ether) to afford the title compound as a yellow oil.

Intermediate 119 (S)-5-Bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 118 substituting (S)-1-cyclopropyl-2,2,2-trifluoroethanamine for 1-cyclopropyl-2,2,2-trifluoroethanamine in Step A.

Intermediate 120 5-Bromo-4-(difluoromethyl)-N-(4,4,4-trifluoro-2-methylbutan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 118 substituting 4,4,4-trifluoro-2-methylbutan-2-amine for 1-cyclopropyl-2,2,2-trifluoroethanamine in Step A.

Intermediate 121: Step A (R)-4-(Difluoromethyl)-N-(3-methylbutan-2-yl)pyridin-2-amine

2-Chloro-4-(difluoromethyl)pyridine (2.0 g, 12 mmol) and (R)-3-methylbutan-2-amine (4.3 g, 49 mmol) were added to a 30 mL microwave tube. The resultant mixture was stirred while heating at 180° C. for 16 hours and at 200° C. for another 16 hours before cooling to room temperature and concentrating to dryness under reduced pressure to give the crude product, which was purified by FCC (0-10% ethyl acetate/petroleum ether) to afford the title compound as a yellow oil.

Intermediate 121: Step B (R)-5-Bromo-4-(difluoromethyl)-N-(3-methylbutan-2-yl)pyridin-2-amine

NBS (1.52 g, 8.54 mmol) was added in portions to a 0° C. (ice/water) solution consisting of (R)-4-(difluoromethyl)-N-(3-methylbutan-2-yl)pyridin-2-amine (1.83 g, 8.54 mmol, Intermediate 121: Step A) and dichloromethane (30 mL). The resultant mixture was stirred at 0° C. for 1 hour before pouring into water (30 mL) and extracting with dichloromethane (30 mL×3). The combined organic extracts were dried over anhydrous Na₂SO₄, filtered, and concentrated to dryness under reduced pressure to give the crude product, which was purified by FCC (0-10% ethyl acetate/petroleum ether) to afford the title compound as a yellow oil.

Intermediate 122 (R)-5-Bromo-4-(difluoromethyl)-N-(3,3-dimethylbutan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 121 substituting (R)-3,3-dimethylbutan-2-amine for (R)-3-methylbutan-2-amine in Step A.

Intermediate 123 (S)-5-Bromo-4-(difluoromethyl)-N-(3,3-dimethylbutan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 121 substituting (S)-3,3-dimethylbutan-2-amine for (R)-3-methylbutan-2-amine in Step A.

Intermediate 124 (S)-5-Bromo-4-(difluoromethyl)-N-(3-methylbutan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 121 substituting (S)-3-methylbutan-2-amine for (R)-3-methylbutan-2-amine in Step A.

Intermediate 125 5-Bromo-N-(cyclobutylmethyl)-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 121 substituting cyclobutylmethanamine for (R)-3-methylbutan-2-amine in Step A.

Intermediate 126 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylicacid

Ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (1.01 g, 2.08 mmol, Intermediate 107) was diluted with EtOH and water (13 mL, 1:1 v/v) before DIPEA (1.1 mL, 6.3 mmol) was added, and the suspension was stirred at 80° C. for 3 h. After this time, the solution was allowed to cool and its pH was adjusted to pH 4 with 1.0 N aqueous HCl. The resulting mixture was extracted three times with EtOAc, and the organic layers were combined, dried with anhydrous MgSO₄, filtered, and concentrated to afford the title compound.

Intermediate 127: Step A (S)—N-(1-Cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine

A mixture of 2-bromo-4-(difluoromethyl)pyridine (2.0 g, 9.6 mmol), (S)-1-cyclopropyl-2,2,2-trifluoroethanamine (2.2 g, 13 mmol), and NaOt-Bu (2.77 g, 28.9 mmol) in t-amyl alcohol (40 mL) was sparged with argon for 5 min before SPhos Pd G3 (250 mg, 0.289 mmol) was added, and the mixture was sparged with argon for another 5 min. The mixture was then stirred at 95° C. for 15 hours. After this time, the mixture was allowed to cool, diluted with water, and extracted twice with ethyl acetate. The organic layers were combined, dried over anhydrous Na₂SO₄, filtered, and concentrated. The residue was purified by FCC (0-5% EtOAc/petroleum ether) to afford the title compound.

Intermediate 127: Step B (S)-5-Bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine

N-Bromosuccinimide (1.60 g, 8.99 mmol) was added in portions to a solution of (S)—N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (2.40 g, 9.02 mmol, Intermediate 127: Step A) in MeCN (25 mL), and the resulting mixture was stirred at rt for 5 h. The mixture was diluted with water, and then extracted with twice with EtOAc. The organic layers were combined, dried over anhydrous Na₂SO₄, filtered, and concentrated. The residue was purified by FCC (2-20% EtOAc/petroleum ether) to afford the title compound.

Intermediate 128 Ethyl 5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77, substituting (S)-5-bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 127: Step B) and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 129 Ethyl 5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77, substituting (S)-5-bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 127: Step B) and ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 109: Step A) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 130 Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Example 77, substituting (S)-5-bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 127: Step B) and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Intermediate 131 5-Bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 127, substituting 1-methylcyclobutan-1-amine for (S)-1-cyclopropyl-2,2,2-trifluoroethanamine in Step A.

Intermediate 132 N—((R)-3-Hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) and (R)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol.

Intermediate 133 Potassium (S)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) for 5-bromo-N-cyclopentyl-4-(difluoromethyl) pyridin-2-amine.

Intermediate 134 (S)—N-(1,1-Dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72, Step B, substituting potassium (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step B) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid.

Intermediate 135 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 109: Step A) and (R)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol.

Intermediate 136 Ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 109: Step A) for 5-bromo-N-cyclopentyl-4-(difluoromethyl) pyridin-2-amine and (S)-ethyl 4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 137 (R)-5-Bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine

The title compound was prepared as described in Intermediate 127, substituting (R)-1-cyclopropyl-2,2,2-trifluoroethanamine for (S)-1-cyclopropyl-2,2,2-trifluoroethanamine in Step A.

Intermediate 138 (R)-5-Bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine

The title compound was prepared as described in Intermediate 127, substituting (R)-1,1,1-trifluoropropan-2-amine for (S)-1-cyclopropyl-2,2,2-trifluoroethanamine in Step A.

Intermediate 139 N—((S)-3-Hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) and (S)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol.

Intermediate 140 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 109: Step A) and (S)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol.

Intermediate 141 Potassium (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 73: Step B, substituting ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 109: Step A) for ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 142 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 141) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid.

Intermediate 143 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) and (R)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol.

Intermediate 144 Ethyl 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62: Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 145 Potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 73: Step B, substituting ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 144) for ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 146 Potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 73: Step B, substituting ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) for ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 147 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 146) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid.

Intermediate 148 Ethyl 5-(6-(((R)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62: Step A, substituting (R)-5-bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 137) and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 149 Ethyl 5-(4-(difluoromethyl)-6-(((R)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62: Step A, substituting (R)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 138) and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 73: Step A) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 150 Ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)-5-(6-(neopentylamino)-4-(trifluoromethyl) pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting 5-bromo-N-neopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 73: Step A) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 22) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 151 Ethyl (S)-5-(4-(difluoromethyl)-6-(neopentylamino)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting 5-bromo-4-(difluoromethyl)-N-neopentylpyridin-2-amine (Intermediate 73: Step A) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 23) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 152 Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 153 Potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 152) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 154 Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting 5-bromo-N-(tert-butyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 59) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 155 Potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 154) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 156 Potassium (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 157 Potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxylate (Intermediate 96) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 158 Ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting(S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 109: Step A) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 159 Potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 158) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 160 Ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 93 substituting 5-bromo-N-(tert-butyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 59) in place of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate.

Intermediate 161 Potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate. (Intermediate 160) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 162 Potassium (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 110) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 163 Potassium (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 164 Potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 130) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 165 Potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate

The title compound was prepared as described in Intermediate 62, Step B substituting 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 130) for ethyl (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 62, Step A).

Intermediate 166 (R)-4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-(7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) for ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate.

Intermediate 167 (S)-4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazole-2-carboxylate (Intermediate 70: Step A) for ethyl 4-((1R,4R)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate.

Example 1 5-(6-(Cyclohexylamino)-5-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

To an oven-dried vial under N₂ was added 5-bromo-N-cyclohexyl-3-(trifluoromethyl)pyridin-2-amine (100 mg, 0.3 mmol, Intermediate 1) and 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (130 mg, 0.40 mmol, Intermediate 65: Step C). To this mixture was added pivalic acid (16 mg, 0.21 mmol), KOAc (77 mg, 0.84 mmol), palladium(II) acetate (5.0 mg, 0.022 mmol), and 2-dicyclohexylphosphino-2′,6′-di-1-propoxy-1,1′-biphenyl (19 mg, 0.044 mmol), in that order, followed by butyronitrile (2 mL) that was sparged with nitrogen for 90 minutes in a separate flask. The reaction was heated to 120° C. for 18 h. The reaction was cooled to room temperature, poured into a saturated aqueous sodium bicarbonate/water solution (1:1), and extracted with ethyl acetate (3×). The combined organic layers were dried over anhydrous sodium sulfate, and concentrated to dryness. The residue was purified by reverse phase HPLC to give the title compound. MS (ESI): mass calcd. for C₂₆H₃₃F₄N₅O₃S, 571.6; m/z found, 572.1[M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.41 (d, J=2.4 Hz, 1H), 7.81 (dd, J=2.3, 0.9 Hz, 1H), 7.57-7.49 (m, 1H), 5.00 (d, J=7.5 Hz, 1H), 4.96-4.88 (m, 0.5H), 4.84-4.76 (m, 0.5H), 4.13-4.06 (m, 2H), 3.65-3.54 (m, 1H), 3.46 (d, J=6.3 Hz, 2H), 3.43-3.31 (m, 1H), 3.30-3.21 (m, 1H), 2.10-1.60 (m, 8H), 1.51-1.37 (m, 2H), 1.30 (s, 10.5H), 1.11-1.04 (m, 0.5H).

Example 2 (S)-5-(6-(Cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-N-((1-hydroxycyclopropyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

EDC.HCl (327 mg, 1.71 mmol) was added to a mixture of 1-(aminomethyl)cyclopropanol (74 mg, 0.80 mmol), potassium (S)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (400 mg, 0.80 mmol, Intermediate 62: Step B), HOBt (220 mg, 1.7 mmol), DIPEA (450 uL, 2.5 mmol), and THF (5 mL) in a 25 mL round bottom flask under N₂ at room temperature. The reaction mixture was stirred at room temperature for 16 hours. Saturated aqueous NH₄Cl (20 mL) was added to the reaction which was then extracted with ethyl acetate (20 mL×2). The combined organic extracts were washed with brine (10 mL), dried over anhydrous sodium sulfate and concentrated to dryness. The residue was purified by preparative HPLC to give the title compound as a pale yellow solid. MS (ESI): mass calcd. for C₂₅H₃₁F₂N₅O₃S, 519.6; m/z found, 520.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.74-8.65 (m, 1H), 8.01 (s, 1H), 7.33 (d, J=7.0 Hz, 1H), 7.14-6.79 (m, 1H), 6.73 (s, 1H), 5.53 (s, 1H), 4.26-4.16 (m, 1H), 4.09-3.97 (m, 1H), 3.48-3.41 (m, 4H), 1.98-1.78 (m, 4H), 1.73-1.38 (m, 8H), 1.10 (d, J=6.5 Hz, 2H), 0.90 (d, J=6.5 Hz, 1H), 0.63-0.52 (m, 4H).

Example 3 5-(6-(Cyclohexylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

To an oven-dried vial under N₂ was added 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine (242 mg, 0.75 mmol, Intermediate 3), 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (237 mg, 0.72 mmol, Intermediate 65: Step C), palladium pivalate (44 mg, 0.14 mmol), cesium carbonate (232 mg, 0.71 mmol) and DMF (10.0 mL). The reaction was capped and heated at 120° C. for 18 h. There was no product present by LC/MS after 18 h so an additional 0.2 eq. of palladium pivalate was added and the reaction heated for an additional 24 h at 120° C. The reaction was cooled, poured into a 1:1 mixture of saturated aqueous sodium bicarbonate/water and extracted with ethyl acetate (2×). The combined organic layers were dried over anhydrous sodium sulfate and concentrated to dryness. The residue was purified by reverse phase HPLC to give the title compound. MS (ESI): mass calcd. for C₂₆H₃₃F₄N₅O₃S, 571.6; m/z found, 572.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.18 (s, 1H), 7.59-7.55 (m, 1H), 6.60 (s, 1H), 5.01-4.86 (m, 2H), 3.97-3.88 (m, 1H), 3.75-3.31 (m, 6H), 2.11-1.97 (m, 3H), 1.95-1.55 (m, 7H), 1.51-1.35 (m, 2H), 1.31 (s, 9H).

Example 4 (S)-5-(6-(Cyclohexylamino)-5-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclohexyl-3-(trifluoromethyl)pyridin-2-amine (Intermediate 1) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₇H₃₆F₃N₅O₃S, 567.7; m/z found, 568.2[M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.42 (dd, J=12.1, 2.4 Hz, 1H), 7.81 (dd, J=20.5, 2.4 Hz, 1H), 7.62-7.51 (m, 1H), 5.02 (dd, J=29.2, 6.6 Hz, 2H), 4.62 (d, J=13.4 Hz, 0.5H), 4.12-4.04 (m, 1H), 3.77 (dd, J=9.3, 4.0 Hz, 0.5H), 3.46 (d, J=6.3 Hz, 2H), 3.25 (d, J=12.9 Hz, 1H), 3.07-2.80 (m, 1H), 2.14-1.98 (m, 3H), 1.81-1.35 (m, 8H), 1.33-1.03 (m, 14H).

Example 5 (S)-5-(6-(Cyclohexylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₇H₃₆F₃N₅O₃S, 567.7; m/z found, 568.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20 (d, J=15.5 Hz, 1H), 7.59 (d, J=7.0 Hz, 1H), 6.60 (s, 1H), 4.91 (d, J=8.0 Hz, 1.5H), 4.49-4.45 (m, 0.4H), 3.95 (s, 0.4H), 3.67 (s, 1H), 3.47 (dd, J=6.3, 1.4 Hz, 2.6H), 2.98 (t, J=13.4 Hz, 0.6H), 2.82-2.76 (m, 0.6H), 2.11-1.95 (m, 3H), 1.82-1.74 (m, 2H), 1.71-1.35 (m, 7H), 1.35-1.07 (m, 14H).

Example 6 5-(6-(Cyclohexylamino)-5-(difluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclohexyl-3-(difluoromethyl)pyridin-2-amine (Intermediate 4) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.6; m/z found, 554.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.89 (s, 1H), 8.54 (d, J=7.6 Hz, 1H), 8.47 (d, J=2.5 Hz, 1H), 8.40-8.35 (m, 1H), 8.19 (d, J=2.5 Hz, 1H), 4.92 (s, 1H), 4.80 (s, 1H), 4.12 (s, 1H), 3.74-3.63 (m, 2H), 3.39-3.34 (m, 1H), 3.27 (d, J=6.3 Hz, 2H), 3.23-3.19 (m, 1H), 1.94-1.88 (m, 4H), 1.68 (s, 2H), 1.48-1.37 (m, 8H), 1.12 (s, 6H).

Example 7 4-(4-Fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(5-(trifluoromethyl)-6-((3,3,3-trifluoropropyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-3-(trifluoromethyl)-N-(3,3,3-trifluoropropyl)pyridin-2-amine (Intermediate 5) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₃H₂₆F₇N₅O₃S, 585.5; m/z found, 585.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.48-8.44 (m, 1H), 7.87 (dd, J=2.4, 0.9 Hz, 1H), 7.58-7.51 (m, 1H), 5.37 (s, 1H), 4.94-4.91 (m, 0.5H), 4.82-4.79 (m, 0.5H), 4.15-4.06 (m, 1H), 3.85 (q, J=6.3 Hz, 2H), 3.66-3.52 (m, 1H), 3.47 (d, J=6.3 Hz, 2H), 3.44-3.35 (m, 1H), 3.30-3.20 (m, 1H), 2.56-2.45 (m, 2H), 2.05-1.65 (m, 5H), 1.30 (s, 6H).

Example 8 4-(4-Fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(4-(trifluoromethyl)-6-((3,3,3-trifluoropropyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-4-(trifluoromethyl)-N-(3,3,3-trifluoropropyl)pyridin-2-amine (Intermediate 6) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₃H₂₆F₇N₅O₃S, 585.5; m/z found, 585.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.24 (s, 1H), 7.58-7.53 (m, 1H), 6.66 (s, 1H), 5.20 (t, J=6.1 Hz, 1H), 4.92-4.78 (m, 1H), 4.00-3.87 (m, 1H), 3.72 (q, J=6.4 Hz, 2H), 3.60-3.38 (m, 5H), 2.53-2.44 (m, 2H), 1.96-1.69 (m, 5H), 1.32 (s, 6H).

Example 9 5-(6-(Cyclobutylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclobutyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 7) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₂₉F₄N₅O₃S, 543.6; m/z found, 544.0 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.19 (s, 1H), 7.58-7.52 (m, 1H), 6.56 (s, 1H), 5.23 (d, J=6.9 Hz, 1H), 4.83-4.74 (m, 1H), 4.22 (q, J=7.7 Hz, 1H), 3.92 (d, J=13.2 Hz, 1H), 3.60-3.34 (m, 5H), 2.54-2.38 (m, 2H), 2.02-1.63 (m, 9H), 1.31 (s, 6H).

Example 10 5-(6-(Cyclopentylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 8) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₁F₄N₅O₃S, 557.6; m/z found, 558.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.19 (s, 1H), 7.59-7.53 (m, 1H), 6.64 (s, 1H), 5.04 (d, J=6.9 Hz, 1H), 4.92-4.78 (m, 1H), 4.08 (q, J=6.4 Hz, 1H), 3.92 (d, J=13.0 Hz, 1H), 3.62-3.34 (m, 5H), 2.17-2.00 (m, 2H), 1.98-1.61 (m, 9H), 1.56-1.43 (m, 2H), 1.31 (s, 6H).

Example 11 (S)-5-(6-(Cyclohexylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.6; m/z found, 590.3 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.13 (s, 1H), 7.50 (d, J=7.7 Hz, 1H), 6.59 (s, 1H), 4.89 (d, J=7.9 Hz, 1H), 4.75-4.65 (m, 0.3H), 4.51-4.46 (m, 0.7H), 4.13-4.01 (m, 1H), 3.94-3.82 (m, 1H), 3.67 (s, 1H), 3.56-3.44 (m, 2H), 2.57-2.52 (m, 1H), 2.22-1.97 (m, 3H), 1.89 (s, 1H), 1.80-1.75 (m, 2H), 1.71-1.60 (m, 1H), 1.51-1.15 (m, 14H).

Example 12 4-(4-Fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-(isopropylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-isopropyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 11) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₃H₂₉F₄N₅O₃S, 531.6; m/z found, 532.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20 (s, 1H), 7.58-7.53 (m, 1H), 6.61 (s, 1H), 4.95-4.74 (m, 2H), 4.09-3.86 (m, 2H), 3.60-3.34 (m, 5H), 1.96-1.63 (m, 5H), 1.38-1.19 (m, 12H).

Example 13 5-(6-((3,3-Difluorocyclohexyl)amino)-5-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(3,3-difluorocyclohexyl)-3-(trifluoromethyl)pyridin-2-amine (Intermediate 27) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₁F₆N₅O₃S, 607.6; m/z found, 608.3 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.45-8.42 (m, 1H), 7.86-7.82 (m, 1H), 7.56-7.52 (m, 1H), 5.29 (s, 1H), 4.94-4.90 (m, 1H), 4.84-4.80 (m, 1H), 4.58-4.52 (m, 1H), 4.17-4.04 (m, 1H), 3.62-3.56 (m, 1H), 3.47 (d, J=6.3 Hz, 2H), 3.41-3.37 (m, 1H), 3.29-3.24 (m, 1H), 2.46-2.40 (m, 1H), 2.08-1.78 (m, 8H), 1.78-1.48 (m, 3H), 1.30 (s, 6H).

Example 14 5-(6-(Cyclohexylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclohexyl-4-(difluoromethyl)pyridin-2-amine (Intermediate 15) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.6; m/z found, 554.3 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.04 (s, 1H), 7.58-7.54 (m, 1H), 6.85-6.63 (m, 1H), 6.60 (s, 1H), 4.92-4.75 (m, 2H), 3.97-3.93 (m, 1H), 3.67 (br s, 1H), 3.57-3.31 (m, 5H), 2.06-2.01 (m, 2H), 1.95 (s, 1H), 1.92-1.62 (m, 7H), 1.49-1.36 (m, 2H), 1.31 (s, 9H).

Example 15 5-(6-(Cyclohexylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4,4-difluoropiperidine-1-carbonyl)-N-(3-hydroxy-3-methylbutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 4-(4,4-difluoropiperidine-1-carbonyl)-N-(3-hydroxy-3-methylbutyl)thiazole-2-carboxamide (Intermediate 71) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₇H₃₄F₅N₅O₃S, 603.7; m/z found, 603.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17 (s, 1H), 7.97-7.93 (m, 1H), 6.59 (s, 1H), 4.92 (d, J=7.9 Hz, 1H), 3.77-3.74 (m, 2H), 3.66-3.62 (m, 3H), 3.54-3.51 (m, 2H), 2.09-1.86 (m, 6H), 1.83-1.76 (m, 4H), 1.69-1.63 (m, 1H), 1.55 (s, 1H), 1.51-1.36 (m, 2H), 1.33 (s, 6H), 1.31-1.17 (m, 3H).

Example 16 5-(6-((3,3-Difluorocyclobutyl)amino)-5-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(3,3-difluorocyclobutyl)-3-(trifluoromethyl)pyridin-2-amine (Intermediate 28) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₂₇F₆N₅O₃S, 579.6; m/z found, 580.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.23 (s, 1H), 7.57-7.53 (m, 1H), 6.61 (s, 1H), 5.35 (d, J=6.0 Hz, 1H), 4.97-4.87 (m, 1H), 4.93-4.91 (m, 0.5H), 4.83-4.81 (m, 0.5H), 4.24 (d, J=8.6 Hz, 1H), 3.99-3.86 (m, 1H), 3.60-3.41 (m, 5H), 3.14-3.06 (m, 2H), 2.61-2.44 (m, 2H), 1.95-1.73 (m, 4H), 1.32 (d, J=1.7 Hz, 6H).

Example 17 (S)-5-(6-(Cyclohexylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)—N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 72: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₈H₃₆F₃N₅O₄S₂, 627.8; m/z found, 628.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19 (d, J=20.1 Hz, 1H), 7.22 (dd, J=16.1, 7.9 Hz, 1H), 6.62 (s, 1H), 4.92 (d, J=8.0 Hz, 1.5H), 4.47 (d, J=13.6 Hz, 0.4H), 4.26-4.21 (m, 1H), 3.88 (s, 0.4H), 3.68 (s, 1H), 3.37 (d, J=13.2 Hz, 0.6H), 3.22-3.07 (m, 4H), 2.94 (t, J=13.3 Hz, 0.6H), 2.79 (t, J=13.3 Hz, 0.4H), 2.42 (dd, J=9.8, 5.4 Hz, 2H), 2.30 (s, 2H), 2.08-1.97 (m, 2H), 1.80-1.75 (m, 2H), 1.71-0.99 (m, 15H).

Example 18 5-(6-((4,4-Difluorocyclohexyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(4,4-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 29) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₁F₆N₅O₃S, 607.6; m/z found, 608.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.22 (s, 1H), 7.57-7.53 (m, 1H), 6.63 (s, 1H), 4.94-4.87 (m, 0.5H), 4.85-4.78 (t, J=7.7 Hz, 1.5H), 3.99-3.88 (m, 2H), 3.61-3.37 (m, 5H), 2.23-2.07 (m, 4H), 1.96-1.70 (m, 7H), 1.66-1.56 (q, J=14.3, 12.1 Hz, 2H), 1.32 (s, 6H).

Example 19 (S)-5-(6-(Cyclohexylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.6; m/z found, 554.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.17 (s, 1H), 7.59-7.52 (m, 1H), 6.58 (s, 1H), 4.88 (d, J=7.7 Hz, 1H), 4.33-4.17 (m, 1H), 3.72-3.36 (m, 5H), 2.10-1.97 (m, 4H), 1.97-1.82 (m, 2H), 1.81-1.70 (m, 3H), 1.68-1.62 (m, 2H), 1.61-1.49 (m, 1H), 1.47-1.37 (m, 2H), 1.35-1.17 (m, 9H), 1.11 (d, J=6.4 Hz, 1H).

Example 20 5-(6-((3,3-Difluorocyclopentyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(3,3-difluorocyclopentyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 30) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₂₉F₆N₅O₃S, 593.6; m/z found, 594.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.21 (s, 1H), 7.59-7.52 (m, 1H), 6.61 (s, 1H), 5.28 (d, J=7.1 Hz, 1H), 4.93-4.90 (m, 0.5H), 4.83-4.80 (m, 0.5H), 4.49-4.43 (m, 1H), 3.95-3.90 (m, 1H), 3.61-3.38 (m, 5H), 2.71-2.55 (m, 1H), 2.39-2.22 (m, 2H), 2.21-1.94 (m, 3H), 1.93-1.71 (m, 5H), 1.32 (s, 6H).

Example 21 5-(6-((3,3-Difluorocyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(3,3-difluorocyclobutyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 31) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₂₇F₆N₅O₃S, 579.6; m/z found, 580.0 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.21 (s, 1H), 7.58-7.52 (m, 1H), 6.58 (s, 1H), 5.49 (d, J=6.0 Hz, 1H), 4.94-4.90 (m, 0.5H), 4.84-4.80 (m, 0.5H), 4.31-4.18 (m, 1H), 3.95-3.90 (m, 1H), 3.58-3.46 (m, 5H), 3.16-3.00 (m, 2H), 2.58-2.46 (m, 2H), 1.97-1.72 (m, 5H), 1.32 (s, 6H).

Example 22 5-(6-((6,6-Difluorospiro[3.3]heptan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(6,6-difluorospiro[3.3]heptan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 33) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₇H₃₁F₆N₅O₃S, 619.6; m/z found, 620.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20 (s, 1H), 7.58-7.51 (m, 1H), 6.56 (s, 1H), 5.14 (d, J=6.6 Hz, 1H), 4.94-4.89 (m, 0.5H), 4.82-4.78 (m, 0.5H), 4.26-4.20 (m, 1H), 3.94-3.88 (m, 1H), 3.60-3.37 (m, 5H), 2.77-2.51 (m, 6H), 2.12-2.04 (m, 2H), 1.90 (s, 5H), 1.32 (s, 6H).

Example 23 5-(6-((3,3-Difluorocyclohexyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(3,3-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 32) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₁F₆N₅O₃S, 607.6; m/z found, 608.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.22 (s, 1H), 7.58-7.52 (m, 1H), 6.64 (s, 1H), 5.04 (d, J=8.1 Hz, 1H), 4.94-4.90 (m, 0.5H), 4.81-4.78 (m, 0.5H), 4.22 (s, 1H), 3.94-3.89 (m, 1H), 3.60-3.37 (m, 5H), 2.45-2.40 (m, 1H), 2.11-1.63 (m, 11H), 1.50-1.31 (m, 1H), 1.32 (s, 6H).

Example 24 4-(4-Fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-(spiro[3.3]heptan-2-ylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(spiro[3.3]heptan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 34) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₇H₃₃F₄N₅O₃S, 583.7; m/z found, 584.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19 (s, 1H), 7.59-7.52 (m, 1H), 6.54 (s, 1H), 5.14 (d, J=6.6 Hz, 1H), 4.93-4.87 (m, 0.5H), 4.83-4.77 (m, 0.5H), 4.09-4.02 (m, 1H), 3.94-3.85 (m, 1H), 3.59-3.36 (m, 5H), 2.58-2.50 (m, 2H), 2.14-2.05 (m, 2H), 2.00-1.93 (m, 2H), 1.93-1.64 (m, 9H), 1.31 (s, 6H).

Example 25 (S)-5-(6-(Cyclohexylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylazetidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylazetidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 68) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10 (d, J=7.6 Hz, 1H), 7.57-7.48 (m, 1H), 6.59 (s, 1H), 4.91-4.87 (m, 1.3H), 4.60-4.43 (m, 1.3H), 4.28-4.22 (m, 0.7H), 4.12-3.93 (m, 0.8H), 3.65 (s, 1H), 3.54-3.41 (m, 2H), 2.55-2.40 (m, 1H), 2.03 (d, J=11.7 Hz, 2H), 1.98-1.53 (m, 3H), 1.51-1.12 (m, 16H).

Example 26 5-(6-((2,2-Difluorocyclohexyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(2,2-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 47) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₁F₆N₅O₃S, 607.6; m/z found, 608.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.25-8.19 (m, 1H), 7.60-7.51 (m, 1H), 6.74 (s, 1H), 5.10 (t, J=8.3 Hz, 1H), 4.89 (s, 0.5H), 4.79 (s, 0.5H), 4.40 (s, 1H), 3.94 (t, J=15.1 Hz, 1H), 3.59-3.33 (m, 5H), 2.28-2.18 (m, 1H), 2.10 (s, 1H), 1.96 (s, 1H), 1.92-1.72 (m, 7H), 1.64-1.41 (m, 3H), 1.31 (s, 6H).

Example 27 (S)-5-(6-(Cyclopentylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 8) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.6; m/z found, 554.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.21 (d, J=19.3 Hz, 1H), 7.60 (br s, 1H), 6.64 (s, 1H), 5.02 (d, J=7.0 Hz, 1H), 4.89 (s, 0.6H), 4.47 (d, J=13.9 Hz, 0.4H), 4.11-4.05 (m, 1H), 3.96 (s, 0.4H), 3.54-3.38 (m, 2.6H), 2.98 (t, J=13.3 Hz, 0.5H), 2.79 (t, J=13.3 Hz, 0.4H), 2.15-1.92 (m, 3H), 1.82-1.37 (m, 11H), 1.31 (s, 6H), 1.25-1.08 (m, 4H).

Example 28 (S)-5-(6-(Cyclopentylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 8) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 72: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₇H₃₄F₃N₅O₄S₂, 613.7; m/z found, 614.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.26-8.15 (m, 1H), 7.25-7.16 (m, 1H), 6.65 (s, 1H), 5.04 (d, J=6.9 Hz, 1H), 4.90 (s, 0.6H), 4.47 (d, J=13.5 Hz, 0.4H), 4.27-4.20 (m, 1H), 4.15-4.05 (m, 1H), 3.88 (s, 0.4H), 3.37 (d, J=13.3 Hz, 0.6H), 3.23-3.06 (m, 4H), 2.95 (t, J=13.1 Hz, 0.6H), 2.79 (t, J=13.4 Hz, 0.4H), 2.46-2.38 (m, 2H), 2.35-2.24 (m, 2H), 2.13-2.04 (m, 2H), 1.82-1.03 (m, 15H).

Example 29 (R)-5-(6-((1-Cyclopropylethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (R)-5-bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 17) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₁F₄N₅O₃S, 557.6; m/z found, 558.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.18 (s, 1H), 7.60-7.52 (m, 1H), 6.62 (s, 1H), 5.02 (d, J=7.5 Hz, 1H), 4.93-4.85 (m, 0.5H), 4.84-4.75 (m, 0.5H), 3.92 (d, J=12.8 Hz, 1H), 3.58-3.37 (m, 6H), 1.96 (s, 1H), 1.92-1.63 (m, 4H), 1.38-1.22 (m, 9H), 0.98-0.90 (m, 1H), 0.58-0.50 (m, 2H), 0.37-0.33 (m, 1H), 0.30-0.27 (m, 1H).

Example 30 (S)-5-(6-((1-Cyclopropylethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 18) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₁F₄N₅O₃S, 557.6; m/z found, 558.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.18 (s, 1H), 7.60-7.51 (m, 1H), 6.62 (s, 1H), 5.01 (d, J=7.5 Hz, 1H), 4.92-4.86 (m, 0.5H), 4.83-4.75 (m, 0.5H), 3.92 (d, J=13.2 Hz, 1H), 3.58-3.36 (m, 6H), 1.95 (s, 1H), 1.90-1.68 (m, 4H), 1.33-1.25 (m, 9H), 0.98-0.90 (m, 1H), 0.55-0.50 (m, 2H), 0.38-0.34 (m, 1H), 0.31-0.27 (m, 1H).

Example 31 5-(6-(((R*)-2,2-Difluorocyclohexyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(2,2-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 47) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak IC, 5 μm, 250×21 mm, Mobile phase: 12% EtOH+0.2% TEA, 88% CO₂, first eluting peak) monitoring elution at 254 nm. MS (ESI): mass calcd. for C₂₇H₃₄F₅N₅O₃S, 603.7; m/z found, 604.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.23 (d, J=22.5 Hz, 1H), 7.67-7.56 (m, 1H), 6.75 (s, 1H), 5.12 (d, J=9.1 Hz, 1H), 4.89 (br s, 0.5H), 4.49-4.38 (m, 1.5H), 3.93 (s, 0.5H), 3.55-3.36 (m, 2.5H), 2.95 (t, J=13.2 Hz, 0.5H), 2.85-2.69 (m, 0.5H), 2.33-2.16 (m, 1H), 2.14-0.99 (m, 23H).

Example 32 5-(6-(((S*)-2,2-Difluorocyclohexyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(2,2-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 47) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak IC, 5 μm, 250×21 mm, Mobile phase: 12% EtOH+0.2% TEA, 88% CO₂, second eluting peak) monitoring elution at 254 nm. MS (ESI): mass calcd. for C₂₇H₃₄F₅N₅O₃S, 603.7; m/z found, 604.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.23 (d, J=15.9 Hz, 1H), 7.66-7.58 (m, 1H), 6.74 (s, 1H), 5.22-5.13 (m, 1H), 4.87 (br s, 0.5H), 4.49-4.38 (m, 1.5H), 3.95 (s, 0.5H), 3.53-3.36 (m, 2.5H), 3.04-2.90 (m, 0.5H), 2.79 (t, J=13.2 Hz, 0.5H), 2.33-2.16 (m, 1H), 2.15-1.00 (m, 23H).

Example 33 N-(2-Hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-((1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 42) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₄H₂₉F₆N₅O₃S, 581.6; m/z found, 582.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.32-8.19 (m, 1H), 7.65-7.55 (m, 1H), 6.80-6.69 (m, 1H), 5.18-4.79 (m, 2.6H), 4.45 (d, J=12.6 Hz, 0.4H), 4.00 (d, J=18.6 Hz, 0.4H), 3.55-3.40 (m, 2.6H), 3.03-2.95 (m, 0.5H), 2.81 (t, J=13.8 Hz, 0.5H), 2.12-1.92 (m, 1H), 1.74-1.01 (m, 18H).

Example 34 (S)-5-(6-(Cyclohexylamino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclohexyl-4-(difluoromethyl)pyridin-2-amine (Intermediate 15) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)-methyl 2,2-dimethyl-3-(4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamido)propanoate (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₇H₃₇F₂N₅O₃S, 549.7; m/z found, 550.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 10.25-10.00 (br s, 1H), 7.73 (d, J=9.0 Hz, 1H), 7.53 (s, 1H), 7.05-6.75 (m, 2H), 4.81 (s, 0.6H), 4.38 (d, J=13.5 Hz, 0.7H), 4.14 (s, 0.8H), 3.63 (d, J=13.6 Hz, 0.7H), 3.56-3.38 (m, 3H), 3.19 (t, J=13.0 Hz, 0.6H), 2.85 (t, J=12.7 Hz, 0.5H), 2.03 (d, J=11.7 Hz, 2H), 1.93-1.80 (m, 2H), 1.79-1.14 (m, 21H).

Example 35 5-(6-(((R*)-2,2-Difluorocyclohexyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(2,2-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 47) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. The pure diastereomer was isolated via chiral SFC (Stationary phase: Chiralpak IA, 5 μm, 250×21 mm, Mobile phase: 10% EtOH+0.2% TEA, 90% CO₂, first eluting peak) monitoring elution at 254 nm. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.6; m/z found, 590.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.19 (s, 1H), 7.65-7.48 (m, 1H), 6.73 (d, J=2.8 Hz, 1H), 5.14 (dd, J=8.5, 5.1 Hz, 1H), 4.47-4.25 (m, 1H), 4.23-4.15 (m, 1H), 3.71-3.30 (m, 4.5H), 3.07 (s, 1.5H), 2.31-0.78 (m, 20H).

Example 36 5-(6-(((S*)-2,2-Difluorocyclohexyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(2,2-difluorocyclohexyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 47) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. The pure diastereomer was isolated via chiral SFC (Stationary phase: Chiralpak IA, 5 μm, 250×21 mm, Mobile phase: 10% EtOH+0.2% TEA, 90% CO₂, second eluting peak) monitoring elution at 254 nm. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.6; m/z found, 590.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.19 (s, 1H), 7.65-7.48 (m, 1H), 6.72 (d, J=4.6 Hz, 1H), 5.16 (dd, J=19.2, 9.1 Hz, 1H), 4.47-4.25 (m, 1H), 4.23-4.15 (m, 1H), 3.67-3.29 (m, 4.5H), 3.08 (s, 1.5H), 2.36-0.73 (m, 20H).

Example 37 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 20) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₅F₂N₅O₃S, 535.7; m/z found, 536.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.03 (s, 1H), 7.66-7.53 (m, 1H), 6.62 (s, 2H), 4.92 (d, J=7.6 Hz, 1.5H), 4.44 (d, J=13.2 Hz, 0.5H), 3.90 (s, 0.5H), 3.55-3.31 (m, 3.5H), 2.99 (t, J=13.1 Hz, 0.5H), 2.79 (t, J=13.0 Hz, 0.5H), 2.00 (d, J=27.5 Hz, 1H), 1.76-1.23 (m, 14H), 1.15 (dd, J=22.5, 7.0 Hz, 4H), 0.99-0.90 (m, 1H), 0.62-0.45 (m, 2H), 0.39-0.26 (m, 2H).

Example 38 (S)-5-(6-(Cyclopentylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 8) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17 (s, 1H), 7.61-7.55 (m, 1H), 6.62 (s, 1H), 5.12-5.02 (m, 1H), 4.40-3.98 (m, 2H), 3.64-3.35 (m, 4H), 2.20-1.41 (m, 12H), 1.40-1.19 (m, 9H), 1.11 (d, J=6.4 Hz, 1H).

Example 39 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 18) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.6; m/z found, 554.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.19 (d, J=15.3 Hz, 1H), 7.60 (d, J=7.3 Hz, 1H), 6.62 (s, 1H), 5.00 (d, J=7.6 Hz, 1H), 4.89 (s, 0.6H), 4.47 (d, J=13.4 Hz, 0.4H), 3.96 (s, 0.4H), 3.57-3.32 (m, 3.6H), 2.98 (t, J=13.3 Hz, 0.6H), 2.79 (t, J=13.3 Hz, 0.4H), 2.10-2.01 (m, 1H), 1.79-1.05 (m, 18H), 0.99-0.90 (m, 1H), 0.64-0.43 (m, 2H), 0.43-0.22 (m, 2H).

Example 40 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 18) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS(ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.15 (d, J=2.0 Hz, 1H), 7.65-7.49 (m, 1H), 6.60 (s, 1H), 5.02-4.98 (m, 1H), 4.30-4.20 (m, 1H), 3.65-3.32 (m, 5H), 2.14-1.99 (m, 1.6H), 1.99-1.45 (m, 2.4H), 1.40-1.17 (m, 12H), 1.11 (d, J=6.4 Hz, 1H), 0.97-0.93 (m, 1H), 0.61-0.45 (m, 2H), 0.42-0.23 (m, 2H).

Example 41 (S)-5-(6-(Cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine (Intermediate 19) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₅F₂N₅O₃S, 535.7; m/z found, 536.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.05 (s, 1H), 7.68-7.54 (m, 1H), 6.81-6.64 (m, 2H), 4.97 (d, J=7.0 Hz, 1H), 4.89 (s, 0.5H), 4.44 (d, J=12.6 Hz, 0.5H), 4.10-4.06 (m, 1H), 3.90 (s, 0.5H), 3.50-3.44 (m, 2H), 3.37 (d, J=13.2 Hz, 0.5H), 3.05-2.92 (m, 0.5H), 2.79 (t, J=13.0 Hz, 0.5H), 2.21-1.98 (m, 3H), 1.86-1.38 (m, 11H), 1.30 (s, 6H), 1.21-1.09 (m, 4H).

Example 42 (S)-5-(6-(Cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine (Intermediate 19) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.6; m/z found, 522.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.01 (d, J=19.2 Hz, 1H), 7.59-7.53 (m, 1H), 7.02-6.37 (m, 2H), 4.94 (t, J=7.0 Hz, 1H), 4.34-4.16 (m, 1H), 4.09-4.00 (m, 1H), 3.65-3.32 (m, 4H), 2.15-1.41 (m, 13H), 1.32 (d, J=1.6 Hz, 6H), 1.23 (d, J=6.3 Hz, 2H), 1.02 (d, J=6.4 Hz, 1H).

Example 43 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 20) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS(ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.6; m/z found, 522.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 7.99 (d, J=19.4 Hz, 1H), 7.59-7.53 (m, 1H), 7.00-6.57 (m, 2H), 4.93 (dd, J=7.4, 2.2 Hz, 1H), 4.34-4.15 (m, 1H), 3.65-3.33 (m, 5H), 2.13-1.50 (m, 5H), 1.38-1.20 (m, 11H), 1.06-0.88 (m, 2H), 0.60-0.45 (m, 2H), 0.40-0.23 (m, 2H).

Example 44 (S)-5-(6-(Cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine (Intermediate 19) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₁F₄N₅O₃S, 557.6; m/z found, 558.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.00 (d, J=9.2 Hz, 1H), 7.53-7.50 (m, 1H), 6.91-6.56 (m, 2H), 4.97 (d, J=6.9 Hz, 1H), 4.70-4.66 (m, 0.3H), 4.58-4.44 (m, 0.7H), 4.16-3.98 (m, 2H), 3.95-3.85 (m, 1H), 3.60-3.39 (m, 2H), 2.71-2.44 (m, 1H), 2.23-1.59 (m, 8H), 1.59-1.43 (m, 2H), 1.42-1.15 (m, 9H).

Example 45 N-(2-Hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-(((R)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (R)-5-bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 43) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₄H₂₉F₆N₅O₃S, 581.6; m/z found, 582.0 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.26 (d, J=5.6 Hz, 1H), 7.65-7.55 (m, 1H), 6.72 (d, J=13.6 Hz, 1H), 5.20-4.79 (m, 2.6H), 4.46 (d, J=13.3 Hz, 0.4H), 4.03 (s, 0.4H), 3.51-3.47 (m, 2.6H), 3.01 (t, J=13.3 Hz, 0.6H), 2.81 (t, J=13.2 Hz, 0.4H), 2.04-1.93 (m, 1H), 1.77-1.03 (m, 18H).

Example 46 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine (Intermediate 19) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₃S, 533.6; m/z found, 534.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.03 (s, 1H), 7.63-7.56 (m, 1H), 6.91-6.64 (m, 2H), 4.97 (d, J=7.0 Hz, 1H), 4.68 (t, J=4.5 Hz, 1H), 4.28 (t, J=4.6 Hz, 1H), 4.07 (h, J=6.5 Hz, 1H), 3.48 (d, J=6.3 Hz, 2H), 2.17-2.00 (m, 3H), 1.86-1.38 (m, 14H), 1.32 (s, 6H).

Example 47 N-(2-Hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 44) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₄H₂₉F₆N₅O₃S, 581.6; m/z found, 582.0 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.27 (d, J=16.3 Hz, 1H), 7.60 (d, J=6.4 Hz, 1H), 6.76 (s, 1H), 5.08-4.82 (m, 2.6H), 4.45 (d, J=13.6 Hz, 0.4H), 3.98 (s, 0.4H), 3.57-3.39 (m, 2.6H), 2.98 (t, J=13.2 Hz, 0.6H), 2.80 (t, J=13.2 Hz, 0.4H), 2.06-1.97 (m, 1H), 1.75-1.03 (m, 18H).

Example 48 5-(6-(((R)-1-Cyclopropylethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (R)-5-bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 17) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS(ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17-8.14 (m, 1H), 7.60-7.52 (m, 1H), 6.61 (s, 1H), 4.97 (d, J=7.3 Hz, 1H), 4.37-4.16 (m, 1H), 3.67-3.31 (m, 5H), 2.13-1.47 (m, 4H), 1.38-1.20 (m, 12H), 1.11 (d, J=6.4 Hz, 1H), 0.98-0.90 (m, 1H), 0.62-0.44 (m, 2H), 0.36-0.27 (m, 2H).

Example 49 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-((1-hydroxycyclobutyl)methyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 18) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 73: Step C) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₂F₃N₅O₃S, 551.6; m/z found, 552.0 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.15 (s, 1H), 7.64-7.48 (m, 1H), 6.60 (s, 1H), 5.02-4.96 (m, 1H), 4.35-4.15 (m, 1H), 3.75-3.32 (m, 5H), 2.73-2.62 (m, 1H), 2.25-1.45 (m, 9H), 1.35-1.16 (m, 6.2H), 1.09 (d, J=6.5 Hz, 0.8H), 1.02-0.85 (m, 1H), 0.63-0.44 (m, 2H), 0.42-0.22 (m, 2H).

Example 50 5-(6-(((R)-1-Cyclopropylethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (R)-5-bromo-N-(1-cyclopropylethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 21) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS(ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.6; m/z found, 522.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.02-7.97 (m, 1H), 7.62-7.49 (m, 1H), 7.04-6.52 (m, 2H), 4.95-4.89 (m, 1H), 4.36-4.15 (m, 1H), 3.66-3.32 (m, 5H), 2.14-1.45 (m, 5H), 1.37-1.19 (m, 11H), 1.02 (d, J=6.4 Hz, 1H), 1.03-0.91 (m, 1H), 0.62-0.43 (m, 2H), 0.41-0.22 (m, 2H).

Example 51 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropylethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 18) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₂F₃N₅O₃S, 551.6; m/z found, 552.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.14 (s, 1H), 7.63-7.56 (m, 1H), 6.61 (s, 1H), 4.98 (d, J=7.5 Hz, 1H), 4.68 (s, 1H), 4.34 (s, 1H), 3.48 (d, J=6.3 Hz, 2H), 3.40 (p, J=7.0 Hz, 1H), 2.01 (s, 1H), 1.85-1.59 (s, 4H), 1.50-1.40 (m, 4H), 1.38-1.22 (m, 9H), 0.97-0.90 (m, 1H), 0.61-0.45 (m, 2H), 0.41-0.21 (m, 2H).

Example 52 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 41: Step B) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₄H₃₂F₃N₅O₃S, 527.6; m/z found, 528.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.18 (s, 1H), 7.65-7.49 (m, 1H), 6.63 (s, 1H), 4.86 (s, 1H), 4.33-4.18 (m, 1H), 3.65-3.34 (m, 4H), 2.12-1.99 (m, 1.5H), 1.98-1.81 (m, 1.5H), 1.78-1.70 (m, 1H), 1.65-1.46 (s, 10H), 1.36-1.19 (m, 8H), 1.11 (d, J=6.4 Hz, 1H).

Example 53 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(cyclopentylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-cyclopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 8) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₂F₃N₅O₃S, 551.6; m/z found, 552.2 [M+H]⁺. ¹H NMR (600 MHz, CDCl₃) δ 8.16 (s, 1H), 7.63-7.57 (m, 1H), 6.63 (s, 1H), 5.03 (d, J=6.8 Hz, 1H), 4.68 (s, 1H), 4.33 (d, J=5.2 Hz, 1H), 4.10-4.03 (m, 1H), 3.48 (d, J=6.3 Hz, 2H), 2.15-1.98 (m, 3H), 1.83-1.57 (m, 7H), 1.56-1.39 (m, 6H), 1.32 (s, 7H).

Example 54 N-(2-Hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-(((R)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (R)-5-bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 43) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS(ESI): mass calcd. for C₂₃H₂₇F₆N₅O₃S, 567.6; m/z found, 568.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.22-8.20 (m, 1H), 7.59-7.50 (m, 1H), 6.74-6.72 (m, 1H), 5.15-4.85 (m, 2H), 4.42-4.35 (m, 0.3H), 4.20-4.15 (m, 0.7H), 3.68-3.40 (m, 4H), 2.13-1.72 (m, 4H), 1.71-1.50 (m, 1H), 1.43-1.39 (m, 3H), 1.32 (s, 6H), 1.25-1.17 (m, 3H).

Example 55 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropylethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 20) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₃S, 533.6; m/z found, 534.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.01 (s, 1H), 7.63-7.56 (m, 1H), 6.91-6.62 (m, 2H), 4.92 (d, J=7.6 Hz, 1H), 4.68 (t, J=4.7 Hz, 1H), 4.28 (t, J=4.6 Hz, 1H), 3.48 (d, J=6.3 Hz, 2H), 3.45-3.35 (m, 1H), 2.02 (s, 1H), 1.83-1.72 (m, 2H), 1.65-1.55 (m, 2H), 1.49-1.40 (m, 4H), 1.36-1.22 (m, 9H), 0.97-0.91 (m, 1H), 0.62-0.43 (m, 2H), 0.40-0.21 (m, 2H).

Example 56 (S)-5-(6-((2-Cyclopropylpropan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting 5-bromo-N-(2-cyclopropylpropan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 45) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS(ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.6; m/z found, 554.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17 (s, 1H), 7.61-7.52 (m, 1H), 6.81-6.79 (m, 1H), 5.07 (s, 1H), 4.35-4.14 (m, 1H), 3.55-3.45 (m, 4H), 2.13-1.44 (m, 5H), 1.40-1.19 (m, 15.2H), 1.11 (d, J=6.6 Hz, 0.8H), 0.58-0.37 (m, 4H).

Example 57 5-(4-Cyano-6-(cyclohexylamino)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

To a 50 mL round-bottomed flask under N₂ was added 5-bromo-2-(cyclohexylamino)isonicotinonitrile (100 mg, 0.36 mmol, Intermediate 14), 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (130 mg, 0.40 mmol, Intermediate 65: Step C), hexakis(acetato)tripalladium (17 mg, 0.075 mmol), n-butyldi-1-adamantylphosphine (26 mg, 0.075 mmol), pivalic acid (15 mg, 0.15 mmol), K₂CO₃ (200 mg, 1.45 mmol) and DMA (5 mL) and the mixture was then stirred at 110° C. overnight. The reaction mixture was then diluted with water (5 mL) and extracted with ethyl acetate (3×5 mL). The combined organic phases were washed with saturated aqueous sodium chloride solution (3×10 mL), dried over anhydrous sodium sulfate and concentrated to dryness. The residue was purified by reverse-phase prep-HPLC to give the title compound as a yellow solid, MS (ESI): mass calcd. for C₂₆H₃₃FN₆O₃S, 528.6; m/z found, 529.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.40-8.33 (m, 1H), 8.20 (s, 1H), 7.50 (d, J=7.7 Hz, 1H), 6.95 (s, 1H), 4.97-4.85 (m, 1H), 4.71 (s, 1H), 3.82-3.62 (m, 2H), 3.63-3.50 (m, 2H), 3.47-3.38 (m, 1H), 3.29 (d, J=6.2 Hz, 2H), 1.91-1.83 (m, 4H), 1.77-1.57 (m, 5H), 1.38-1.18 (m, 5H), 1.13 (s, 6H).

Example 58 5-(5-Cyano-6-(cyclohexylamino)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-2-(cyclohexylamino)nicotinonitrile (Intermediate 9) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₆H₃₃FN₆O₃S, 528.6; m/z found, 529.1 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.42 (d, J=2.5 Hz, 1H), 8.40-8.33 (m, 1H), 8.05 (d, J=2.5 Hz, 1H), 7.31 (d, J=7.9 Hz, 1H), 4.94-4.82 (m, 1H), 4.69 (s, 1H), 4.07-3.93 (m, 1H), 3.79-3.69 (m, 1H), 3.66-3.57 (m, 1H), 3.31 (s, 1H), 3.28-3.27 (m, 2H), 3.24-3.14 (m, 1H), 1.99-1.79 (m, 3H), 1.79-1.59 (m, 5H), 1.51-1.23 (m, 5H), 1.18-1.08 (m, 7H).

Example 59 5-(6-(Cyclohexylamino)-5-methoxypyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-N-cyclohexyl-3-methoxypyridin-2-amine (Intermediate 10) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₆H₃₆FN₅O₄S, 533.7; m/z found, 534.1 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.38-8.32 (m, 1H), 7.82-7.75 (m, 1H), 7.08 (s, 1H), 6.39 (s, 1H), 4.91-4.79 (m, 1H), 3.89 (s, 1H), 3.84 (s, 3H), 3.81-3.71 (m, 1H), 3.70-3.59 (m, 1H), 3.40-3.27 (m, 4H), 3.20-3.09 (m, 1H), 1.86 (br s, 3H), 1.78-1.55 (m, 5H), 1.51-1.23 (m, 5H), 1.21-1.02 (m, 7H).

Example 60 5-(5-Cyano-6-(cyclohexylamino)-4-methylpyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-2-chloro-4-methylnicotinonitrile (Intermediate 12) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₇H₃₅FN₆O₃S, 542.7; m/z found, 543.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.44-8.38 (m, 1H), 8.16 (s, 1H), 6.99 (d, J=8.0 Hz, 1H), 4.97-4.77 (m, 1H), 4.70 (s, 1H), 4.07-3.91 (m, 1H), 3.65 (s, 1H), 3.53-3.43 (m, 2H), 3.29-3.28 (m, 3H), 2.28 (s, 3H), 1.84-1.71 (m, 6H), 1.66-1.36 (m, 5H), 1.34-1.24 (m, 2H), 1.20-1.06 (m, 7H).

Example 61 (S)-5-(6-(Cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-N-(1,1-dioxidothietan-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 2 substituting 3-aminothietane 1,1-dioxide hydrochloride for 1-(aminomethyl)cyclopropanol. MS (ESI): mass calcd. for C₂₄H₂₉F₂N₅O₄S₂, 553.6; m/z found, 554.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.06-7.97 (m, 1H), 7.85-7.74 (m, 1H), 7.02-6.73 (m, 1H), 6.66-6.62 (m, 1H), 5.05-4.97 (m, 1H), 4.95-4.81 (m, 1H), 4.70-4.55 (m, 2H), 4.28-4.02 (m, 4H), 3.64-3.29 (m, 2H), 2.12-1.89 (m, 4H), 1.84-1.65 (m, 5H), 1.58-1.44 (m, 3H), 1.25-1.18 (m, 2H), 1.00 (d, J=6.5 Hz, 1H).

Example 62 5-(6-(Cyclohexylamino)-5-(difluoromethoxy)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-N-cyclohexyl-3-(difluoromethoxy)pyridin-2-amine (Intermediate 16) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₄S, 569.6; m/z found, 570.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.41-8.33 (m, 1H), 8.10 (d, J=2.1 Hz, 1H), 7.40 (s, 1H), 7.34-6.98 (m, 1H), 6.63 (d, J=8.2 Hz, 1H), 4.91-4.80 (m, 1H), 4.69 (s, 1H), 3.94 (br s, 1H), 3.74 (br s, 1H), 3.68-3.58 (m, 1H), 3.28-3.27 (m, 3H), 3.19-3.11 (m, 1H), 1.95-1.80 (m, 3H), 1.78-1.56 (m, 6H), 1.47-1.23 (m, 5H), 1.11 (s, 6H).

Example 63 5-(6-(Cyclohexylamino)-4-methoxypyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-N-cyclohexyl-4-methoxypyridin-2-amine (Intermediate 26) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₆H₃₆FN₅O₄S, 533.3; m/z: found, 534.1 [M+H]+, ¹H NMR (400 MHz, DMSO-d₆) δ 8.38-8.31 (m, 1H), 7.79 (d, J=1.9 Hz, 1H), 7.08 (s, 1H), 6.39 (s, 1H), 4.91-4.79 (m, 1H), 3.89 (s, 1H), 3.84 (s, 3H), 3.81-3.71 (m, 1H), 3.70-3.59 (m, 1H), 3.28-3.27 (m, 3H), 3.20-3.09 (m, 1H), 1.86 (br s, 3H), 1.78-1.55 (m, 5H), 1.51-1.23 (m, 5H), 1.21-1.02 (m, 7H).

Example 64 5-(6-(Cyclohexylamino)-4-cyclopropylpyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-N-cyclohexyl-4-cyclopropylpyridin-2-amine (Intermediate 36) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂H₃₈FN₅O₃S, 543.2; m/z found, 543.8 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.38-8.31 (m, 1H), 7.82 (s, 1H), 6.65 (d, J=7.8 Hz, 1H), 6.06 (s, 1H), 4.92-4.63 (m, 2H), 3.78-3.63 (m, 2H), 3.56-3.44 (m, 1H), 3.28 (d, J=6.3 Hz, 2H), 3.22-3.12 (m, 1H), 1.88-1.85 (m, 2H), 1.80-1.65 (m, 4H), 1.58-1.50 (m, 3H), 1.38-1.24 (m, 3H), 1.23-1.13 (m, 3H), 1.13-1.11 (m, 7H), 0.96-0.88 (m, 2H), 0.72-0.64 (m, 2H).

Example 65 5-(6-(Cyclohexylamino)-4-isopropylpyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-N-cyclohexyl-4-isopropylpyridin-2-amine (Intermediate 37) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₈H₄₀FN₅O₃S, 545.3; m/z found, 545.8 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.38-8.32 (m, 1H), 7.83 (s, 1H), 6.72 (d, J=7.8 Hz, 1H), 6.47 (s, 1H), 4.89-4.77 (m, 1H), 4.75-4.65 (m, 1H), 3.72-3.65 (m, 2H), 3.51-3.17 (m, 5H), 2.89-2.82 (m, 1H), 1.90-1.87 (m, 2H), 1.73-1.69 (m, 3H), 1.60 (s, 3H), 1.48-1.26 (m, 3H), 1.25-1.15 (m, 3H), 1.14-1.11 (m, 6H), 1.10-1.07 (m, 6H).

Example 66 5-(6-(Cyclohexylamino)-5-fluoro-4-methylpyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-N-cyclohexyl-3-fluoro-4-methylpyridin-2-amine (Intermediate 38) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₆H₃₅F₂N₅O₃S, 535.2; m/z found, 535.8 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.40-8.34 (m, 1H), 7.76 (s, 1H), 6.71 (d, J=6.9 Hz, 1H), 4.94-4.74 (m, 1H), 4.70 (s, 1H), 3.88 (s, 1H), 3.67 (s, 1H), 3.55-3.45 (m, 1H), 3.40-3.37 (m, 1H), 3.28 (d, J=6.3 Hz, 2H), 3.26-3.17 (m, 1H), 2.10 (d, J=2.2 Hz, 3H), 1.86 (s, 3H), 1.73 (s, 3H), 1.63-1.60 (m, 3H), 1.42 (s, 1H), 1.38-1.22 (m, 4H), 1.12 (s, 6H).

Example 67 5-(6-(Cyclohexylamino)-4-methylpyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-N-cyclohexyl-4-methylpyridin-2-amine (Intermediate 35: Step B) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₇H₃₇FN₄O₃S, 516.7; m/z found, 517.9 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.41-8.34 (m, 1H), 7.84 (s, 1H), 6.74 (d, J=7.8 Hz, 1H), 6.39 (s, 1H), 4.90-4.72 (m, 1H), 3.75-3.13 (m, 9H), 2.13 (s, 3H), 1.90-1.87 (m, 2H), 1.82-1.66 (m, 3H), 1.66-1.50 (m, 3H), 1.36-1.27 (m, 3H), 1.25-1.14 (m, 3H), 1.12 (s, 6H).

Example 68 5-(5-Cyano-6-(cyclohexylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting 5-bromo-2-(cyclohexylamino)-4-(trifluoromethyl)nicotinonitrile (Intermediate 61: Step B) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₇H₃₂F₄N₆O₃S, 596.6; m/z found, 597.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.44 (s, 1H), 8.45-8.38 (m, 1H), 7.53 (d, J=7.9 Hz, 1H), 4.97-4.86 (m, 1H), 4.70 (s, 1H), 4.10-3.96 (m, 1H), 3.62-3.41 (m, 4H), 3.28 (d, J=6.2 Hz, 2H), 1.96-1.58 (m, 10H), 1.53-1.45 (m, 2H), 1.35-1.26 (m, 2H), 1.12 (s, 6H).

Example 69 5-(6-(Cyclohexylamino)-4-ethoxypyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

To a 50 mL round bottomed flask under N₂ was added 5-bromo-N-cyclohexyl-4-ethoxypyridin-2-amine (200 mg, 0.68 mmol, Intermediate 39: Step B), 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (250 mg, 0.75 mmol, Intermediate 65: Step C), hexakis(acetato)tripalladium (31 mg, 0.14 mmol), n-butyldi-1-adamantylphosphine (49 mg, 0.14 mmol), pivalic acid (28 mg, 0.27 mmol), K₂CO₃ (376 mg, 2.72 mmol) and DMA (5 mL). The mixture was then stirred at 110° C. for 6 h. The reaction mixture was diluted with water (10 mL) and the aqueous layer was extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with saturated aqueous sodium chloride solution (20 mL), dried over anhydrous sodium sulfate and concentrated to dryness. The residue was purified by prep-HPLC to give the title compound as a yellow solid. MS (ESI): mass calcd. for C₂₇H₃₈FN₅O₄S, 547.3; m/z found, 547.8 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.27-8.20 (m, 1H), 7.86 (s, 1H), 6.83 (d, J=7.6 Hz, 1H), 6.11 (s, 1H), 4.89-4.77 (m, 1H), 4.70 (s, 1H), 4.08 (q, J=6.9 Hz, 2H), 3.73 (s, 2H), 3.62-3.52 (m, 1H), 3.27-3.26 (m, 3H), 3.14-3.10 (m, 1H), 1.90-1.82 (m, 3H), 1.76-1.51 (m, 5H), 1.48-1.25 (m, 6H), 1.23-1.14 (m, 3H), 1.12 (s, 6H).

Example 70 5-(6-(cyclohexylamino)-4-ethylpyridin-3-yl)-4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 69 substituting 5-N-cyclohexyl-4-ethylpyridin-2-amine (Intermediate 40) for 5-bromo-N-cyclohexyl-4-ethoxypyridin-2-amine. MS (ESI) mass calcd for C₂₇H₃₈FN₅O₃S 531.3 m/z: found 531.8 [M+H]+, ¹H NMR (400 MHz, DMSO-d) δ 8.35 (t, J=6.2 Hz, 1H), 7.83 (s, 1H), 6.78 (s, 1H), 6.43 (s, 1H), 4.88-4.76 (m, 1H), 4.70 (s, 1H), 3.81-3.60 (m, 2H), 3.54-3.44 (m, 1H), 3.34 (s, 1H), 3.28 (d, J=6.3 Hz, 2H), 3.23-3.13 (m, 1H), 2.50-2.43 (m, 2H), 1.90-1.88 (m, 2H), 1.79-1.69 (m, 3H), 1.60-1.57 (m, 3H), 1.36-1.27 (m, 3H), 1.23-1.15 (m, 3H), 1.12 (s, 6H), 1.06 (t, J=7.5 Hz, 3H).

Example 71 (S)-5-(6-(Cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

5-Bromo-N-cyclopentyl-4-(difluoromethyl) pyridin-2-amine (150 mg, 0.50 mmol, Intermediate 19), (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (210 mg, 0.65 mmol, Intermediate 73, Step C), Pd(OAc)₂ (11 mg, 0.049 mmol), PCy₃.HBF₄ (37 mg, 0.10 mmol), pivalic acid (20 mg, 0.20 mmol), K₂CO₃ (277 mg, 2.10 mmol), and DMAc (3 mL) were added to a 5 mL microwave tube. The resultant mixture was sparged with Ar for 5 minutes and then stirred at 120° C. in a microwave for 1 hour before cooling to room-temperature and pouring into ethyl acetate (20 mL). The resultant mixture was washed with H₂O (10 mL×2), dried over anhydrous sodium sulfate and concentrated to dryness to give the crude product, which was purified by preparative HPLC. The purified product was suspended in water (10 mL), the mixture frozen using dry ice/acetone, and then lyophilized to dryness to afford the title compound as a white solid. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₃S 533.2, m/z found 534.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃-d) δ 8.06-7.95 (m, 1H), 7.65-7.49 (m, 1H), 7.04-6.72 (m, 1H), 6.69-6.61 (m, 1H), 5.06 (br. s., 1H), 4.33-4.16 (m, 1H), 4.12-4.01 (m, 1H), 3.76-3.53 (m, 3H), 3.49-3.35 (m, 1H), 2.77 (br. s., 1H), 2.23-2.01 (m, 7H), 1.99-1.85 (m, 2H), 1.80-1.69 (m, 6H), 1.58-1.44 (m, 3H), 1.27-1.18 (m, 2H), 1.04-0.96 (m, 1H).

Example 72 5-(6-(Cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-N-((1r,3r)-3-(methylsulfonyl)cyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71 substituting 4-((S)-2-methylpyrrolidine-1-carbonyl)-N-((1r,3r)-3-(methylsulfonyl)cyclobutyl)thiazole-2-carboxamide (Intermediate 74) for (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₄S₂, 581.7; m/z found, 582.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.41-9.27 (m, 1H), 8.00 (s, 1H), 7.39-7.29 (m, 1H), 7.16-6.78 (m, 1H), 6.73 (s, 1H), 4.68-4.56 (m, 1H), 4.25-4.12 (m, 1H), 4.08-3.97 (m, 1H), 3.88-3.77 (d, J=5.0 Hz, 1H), 3.47-3.35 (m, 2H), 2.97 (s, 3H), 2.76-2.62 (m, 4H), 2.01-1.78 (m, 4H), 1.75-1.38 (m, 8H), 1.10 (d, J=6.0 Hz, 2H), 0.87 (d, J=6.5 Hz, 1H).

Example 73 (S)-5-(6-(Cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-N-((3-hydroxyoxetan-3-yl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71 substituting (S)—N-((3-hydroxyoxetan-3-yl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 75) for (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₁F₂N₅O₄S, 535.6; m/z found, 536.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.94-8.81 (m, 1H), 8.01 (s, 1H), 7.34 (d, J=6.6 Hz, 1H), 7.16-6.78 (m, 1H), 6.73 (s, 1H), 5.98-5.88 (m, 1H), 4.55-4.36 (m, 4H), 4.26-3.97 (m, 2H), 3.70-3.42 (m, 4H), 2.01-1.40 (m, 12H), 1.10 (d, J=6.6 Hz, 2H), 0.90 (d, J=6.2 Hz, 1H).

Example 74 5-(6-(Cyclopentylamino)-4-(difluoromethyl)pyridin-3-yl)-N-((1r,3s)-3-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71 substituting N-((1r,3r)-3-((tert-butyldimethylsilyl)oxy)cyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 2: Step B) for (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₁F₂N₅O₃S, 519.6; m/z found, 520.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.16-9.10 (m, 1H), 8.00 (s, 1H), 7.36-7.29 (m, 1H), 7.15-7.01 (m, 1H), 6.93-6.79 (m, 1H), 6.73 (s, 1H), 5.04-5.00 (m, 1H), 4.52-4.44 (m, 1H), 4.35-4.27 (m, 1H), 4.21-3.98 (m, 3H), 2.42-2.38 (m, 2H), 2.23-2.08 (m, 2H), 2.02-1.73 (m, 5H), 1.72-1.36 (m, 7H), 1.09 (d, J=6.5 Hz, 2H), 0.87 (d, J=6.0 Hz, 1H).

Example 75 (S)-5-(6-(Cyclohexylamino)-4-cyclopropylpyridin-3-yl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71 substituting (S)—N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 72: Step D) for (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-cyclohexyl-4-cyclopropylpyridin-2-amine (Intermediate 36) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₃₀H₄₁N₅O₄S₂ 599.3, m/z found 600.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.86-8.64 (m, 1H), 7.82 (s, 1H), 6.30 (d, J=7.5 Hz, 1H), 6.10 (s, 1H), 4.93-4.44 (m, 1H), 4.30-4.10 (m, 1H), 3.81-3.67 (m, 1H), 3.37-3.21 (m, 2H), 3.17-3.10 (m, 2H), 2.95-2.74 (m, 1H), 2.36-2.08 (m, 4H), 1.95-1.12 (m, 17H), 1.05 (d, J 7.0 Hz, 3H), 1.00-0.80 (m, 3H), 0.76-0.59 (m, 2H).

Example 76 (S)-5-(6-(Cyclohexylamino)-4-cyclopropylpyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-cyclohexyl-4-cyclopropylpyridin-2-amine (Intermediate 36) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₉H₄₁N₅O₃S 539.3, m/z found 540.3 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.13-8.01 (m, 1H), 7.83 (s, 1H), 6.34-6.26 (m, 1H), 6.10 (s, 1H), 4.48 (s, 1H), 3.79-3.68 (m, 1H), 3.31 (d, J 6.0 Hz, 2H), 2.90-2.81 (m, 1H), 2.06-1.53 (m, 9H), 1.48-1.19 (m, 10H), 1.16 (s, 6H), 1.07 (d, J 7.0 Hz, 3H), 0.95-0.86 (m, 2H), 0.74-0.63 (m, 2H).

Example 77 (S)—N-(2-Hydroxy-2-methylpropyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

To an oven-dried vial under N₂ was added 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine (90 mg, 0.29 mmol, Intermediate 46), (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (91 mg, 0.29 mmol, Intermediate 69), bis(tri-tert-butylphosphine)palladium (0) (30 mg, 0.06 mmol), potassium carbonate (80 mg, 0.58 mmol) and DMF (2.0 mL, sparged with N₂ for 2 h). The vial was capped and heated at 130° C. for 24 h. The reaction was cooled, poured into saturated aqueous bicarbonate, and extracted with ethyl acetate (3×). The combined organic layers were dried over anhydrous sodium sulfate and concentrated to dryness. The crude residue was dissolved in 1:1 DMSO:MeOH and purified by reverse phase HPLC to provide the title compound. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (600 MHz, CDCl₃) δ 8.17 (s, 1H), 7.60-7.50 (m, 1H), 6.50 (s, 1H), 5.21 (s, 1H), 4.35-4.27 (m, 0.3H), 4.25-4.16 (m, 0.7H), 3.65-3.37 (m, 4H), 2.30-2.25 (m, 2H), 2.19-1.83 (m, 8H), 1.77-1.73 (m, 1H), 1.65-1.51 (m, 2H), 1.36-1.18 (m, 9H), 1.11 (d, J=6.4 Hz, 1H).

Example 78 N-(2-Hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 44) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₃H₂₇F₆N₅O₃S, 567.6; m/z found, 568.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20 (s, 1H), 7.62-7.50 (m, 1H), 6.68-6.64 (m, 1H), 5.55 (d, J=9.2 Hz, 0.7H), 5.32-5.30 (m, 0.3H), 5.07-4.88 (m, 1H), 4.59-4.50 (m, 0.2H), 4.19-4.14 (m, 0.8H), 3.74-3.36 (m, 4H), 2.17-1.47 (m, 4H), 1.45-1.21 (m, 12H), 1.09 (d, J=6.4 Hz, 1H).

Example 79 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 41: Step B) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.2; m/z found, 539.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.19-8.13 (s, 1H), 7.64-7.55 (m, 1H), 6.67-6.60 (s, 1H), 5.00-4.77 (m, 1H), 4.74-4.63 (m, 1H), 4.34-4.21 (m, 1H), 3.52-3.43 (d, J=6.4 Hz, 2H), 2.02-1.96 (s, 1H), 1.84-1.67 (m, 2H), 1.49-1.40 (m, 13H), 1.35-1.23 (m, 8H).

Example 80 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 41: Step B) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₃S, 541.2; m/z found, 541.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.28-8.12 (m, 1H), 7.67-7.54 (m, 1H), 6.69-6.59 (s, 1H), 4.99-4.81 (m, 1.5H), 4.55-4.41 (m, 0.5H), 4.01-3.87 (m, 0.5H), 3.51-3.45 (dd, J 6.2, 1.3 Hz, 2H), 3.44-3.35 (m, 0.5H), 3.02-2.70 (m, 1H), 2.08-1.91 (m, 1H), 1.72-1.57 (m, 2H), 1.50-1.42 (s, 10H), 1.36-1.28 (m, 8H), 1.23-1.04 (m, 4H).

Example 81 (S)—N-(2-Hydroxy-2-methylpropyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.6; m/z found, 554.3 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20 (d, J=15.7 Hz, 1H), 7.66-7.58 (m, 1H), 6.53 (s, 1H), 5.27 (br s, 1H), 4.89 (br s, 0.6H), 4.47 (d, J=13.3 Hz, 0.4H), 3.94 (br s, 0.4H), 3.55-3.36 (m, 2.6H), 3.00-2.75 (m, 1H), 2.35-2.06 (m, 5H), 2.02-1.87 (m, 2H), 1.74-1.04 (m, 18H).

Example 82 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 44) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₄H₂₇F₆N₅O₃S, 579.6; m/z found, 580.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.18 (s, 1H), 7.62-7.55 (m, 1H), 6.69 (s, 1H), 5.37 (d, J=9.3 Hz, 1H), 5.03-4.88 (m, 1H), 4.67 (s, 1H), 4.49 (s, 1H), 3.55-3.45 (m, 2H), 2.03 (s, 1H), 1.65 (s, 3H), 1.56-1.23 (m, 14H).

Example 83 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 41: Step B) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S, 563.2; m/z found, 563.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20-8.10 (s, 1H), 7.57-7.42 (m, 1H), 6.68-6.60 (s, 1H), 5.01-4.39 (m, 2H), 4.20-3.71 (m, 2H), 3.60-3.37 (m, 2H), 2.68-2.42 (m, 1H), 2.22-1.97 (m, 1H), 1.92-1.73 (m, 1H), 1.49-1.44 (s, 9H), 1.39-1.27 (m, 9H).

Example 84 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-(neopentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-neopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 22) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.6; m/z found, 554.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.15 (s, 1H), 7.62-7.56 (m, 1H), 6.66 (s, 1H), 5.06-4.99 (m, 1H), 4.68 (s, 1H), 4.33 (s, 1H), 3.48 (d, J=6.3 Hz, 2H), 3.17 (d, J=6.1 Hz, 2H), 2.01 (s, 1H), 1.82-1.71 (m, 2H), 1.67-1.61 (m, 2H), 1.47-1.41 (m, 4H), 1.32 (s, 6H), 1.00 (s, 9H).

Example 85 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-(neopentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-neopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 22) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₂F₅N₅O₃S, 577.6; m/z found, 578.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.13 (s, 1H), 7.54-7.46 (m, 1H), 6.66 (s, 1H), 5.08-5.00 (m, 1H), 4.73-4.45 (m, 1H), 4.14-3.81 (m, 2H), 3.56-3.42 (m, 2H), 3.20-3.11 (m, 2H), 2.62-2.50 (m, 1H), 2.17-2.00 (m, 1H), 1.93-1.80 (m, 1H), 1.37-1.28 (m, 9H), 1.01 (s, 9H).

Example 86 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)-5-(6-(neopentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-neopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 22) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₆F₃N₅O₃S, 555.7; m/z found, 556.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.25-8.15 (m, 1H), 7.63-7.55 (m, 1H), 6.67 (s, 1H), 5.08-5.01 (m, 1H), 4.93-3.41 (m, 4H), 3.22-3.13 (m, 2H), 3.02-2.74 (m, 1H), 2.08-1.96 (m, 1H), 1.69-1.62 (m, 1H), 1.57-1.50 (m, 2H), 1.44-1.35 (m, 1H), 1.31 (s, 6H), 1.20 (d, J=6.7 Hz, 1H), 1.12 (d, J=6.8 Hz, 2H), 1.00 (s, 9H), 1.59-1.58 (m, 2H).

Example 87 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)-5-(6-(neopentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting 5-bromo-N-neopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 22) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₃S, 541.6; m/z found, 542.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.15 (s, 1H), 7.64-7.54 (m, 1H), 6.67-6.62 (m, 1H), 5.25-5.11 (m, 1H), 4.36-4.16 (m, 1H), 3.58-3.39 (m, 4H), 3.23-3.09 (m, 2H), 2.27-2.15 (m, 1H), 2.09-2.05 (m, 1H), 1.95-1.88 (m, 1H), 1.78-1.75 (m, 1H), 1.58-1.48 (m, 1H), 1.32-1.29 (m, 6H), 1.25-1.23 (m, 2H), 1.10 (d, J=6.4 Hz, 1H), 1.01-0.98 (m, 9H).

Example 88 (S)-5-(6-((2-Cyclopropylpropan-2-yl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 using (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(2-cyclopropylpropan-2-yl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 48) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₇H₃₇F₂N₅O₃S, 549.7; m/z found, 550.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.05 (s, 1H), 7.73-7.60 (m, 1H), 6.91-6.60 (m, 2H), 5.08 (s, 1H), 4.93-4.38 (m, 1H), 3.91-3.31 (m, 3H), 2.96 (s, 2H), 2.89-2.86 (m, 2H), 2.48-2.38 (m, 1H), 1.70-1.59 (m, 1H), 1.57-1.40 (m, 3H), 1.31 (d, J=6.4 Hz, 12H), 1.17-1.09 (m, 3H), 0.53-0.46 (m, 2H), 0.44-0.39 (m, 2H).

Example 89 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.07-8.01 (m, 1H), 7.66-7.59 (m, 1H), 6.90-6.66 (m, 2H), 5.03 (d, J=9.8 Hz, 1H), 4.83-4.73 (m, 1H), 4.70-4.64 (m, 1H), 4.33-4.27 (m, 1H), 3.48 (d, J=6.2 Hz, 2H), 2.96-2.88 (m, 1H), 2.28 (s, 1H), 2.00-1.91 (m, 1H), 1.83-1.77 (m, 1H), 1.65-1.54 (m, 3H), 1.48-1.41 (m, 4H), 1.31 (s, 6H), 1.06-1.01 (m, 3H).

Example 90 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₂₈F₇N₅O₃S, 599.6; m/z found, 600.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.07-8.01 (m, 1H), 7.53-7.46 (m, 1H), 6.84-6.60 (m, 2H), 4.82-4.48 (m, 3H), 4.13-3.81 (m, 2H), 3.57-3.44 (m, 2H), 2.65-2.51 (m, 1H), 2.16-1.94 (m, 2H), 1.90-1.78 (m, 1H), 1.66-1.60 (m, 1H), 1.36 (d, J=6.4 Hz, 2H), 1.34-1.32 (m, 6H), 1.24 (d, J=6.5 Hz, 1H), 1.08-1.03 (m, 3H).

Example 91 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₂F₅N₅O₃S, 577.6; m/z found, 578.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09 (s, 1H), 7.67-7.59 (m, 1H), 6.95-6.63 (m, 2H), 4.96 (d, J=9.8 Hz, 1H), 4.90-4.38 (m, 2H), 3.94-3.31 (m, 3H), 2.99-2.75 (m, 1H), 2.28-2.18 (m, 1H), 2.01-1.94 (m, 1H), 1.68-1.50 (m, 5H), 1.46-1.32 (m, 1H), 1.31 (s, 6H), 1.17 (d, J=6.9 Hz, 1H), 1.09 (d, J=7.1 Hz, 2H), 1.06-1.02 (m, 3H).

Example 92 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S, 563.6; m/z found, 564.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 7.62-7.52 (m, 1H), 7.01-6.67 (m, 2H), 4.92-4.87 (m, 1H), 4.78 (s, 1H), 4.39-4.18 (m, 1H), 3.59-3.36 (m, 4H), 2.09-1.85 (m, 4H), 1.82-1.72 (m, 1H), 1.68-1.51 (m, 2H), 1.31 (s, 6H), 1.22 (d, J=6.3 Hz, 2H), 1.07-1.02 (m, 4H).

Example 93 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(tert-pentylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(difluoromethyl)-N-(tert-pentyl)pyridin-2-amine (Intermediate 50) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₅F₂N₅O₃S, 535.7; m/z found, 536.3 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.04-8.01 (m, 1H), 7.67-7.59 (m, 1H), 6.90-6.60 (m, 2H), 4.80-4.66 (m, 2H), 4.20-4.15 (m, 1H), 3.48 (d, J=6.3 Hz, 2H), 2.96 (s, 1H), 2.88 (s, 1H), 2.19 (s, 1H), 1.87-1.80 (m, 2H), 1.78-1.68 (m, 3H), 1.45-1.41 (m, 3H), 1.39 (s, 6H), 1.31 (s, 6H), 0.90-0.84 (m, 3H).

Example 94 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(tert-pentylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(difluoromethyl)-N-(tert-pentyl)pyridin-2-amine (Intermediate 50) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₃F₄N₅O₃S, 559.6; m/z found, 560.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.04-7.96 (m, 2H), 7.60-7.49 (m, 1H), 6.81-6.56 (m, 2H), 4.80 (s, 1H), 4.68-4.50 (m, 1H), 4.11-3.82 (m, 2H), 3.56-3.42 (m, 2H), 2.96 (s, 3H), 2.90-2.86 (m, 3H), 2.60-2.50 (m, 1H), 2.13-2.04 (m, 1H), 1.86-1.81 (m, 2H), 1.40 (s, 6H), 1.36 (d, J=6.4 Hz, 2H), 1.21 (d, J=6.6 Hz, 1H), 0.92-0.86 (m, 3H).

Example 95 (S)-5-(4-(Difluoromethyl)-6-(tert-pentylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(difluoromethyl)-N-(tert-pentyl)pyridin-2-amine (Intermediate 50) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₇F₂N₅O₃S, 537.7; m/z found, 538.3 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.07-8.01 (m, 1H), 7.65-7.54 (m, 1H), 6.90-6.61 (m, 2H), 4.94-4.42 (m, 2H), 3.90-3.29 (m, 3H), 3.00-2.71 (m, 2H), 2.04-1.92 (m, 1H), 1.88-1.81 (m, 2H), 1.70-1.59 (m, 1H), 1.55-1.46 (m, 2H), 1.40 (s, 6H), 1.31 (s, 6H), 1.17-1.09 (m, 3H), 0.90-0.84 (m, 3H).

Example 96 (S)-5-(4-(Difluoromethyl)-6-(tert-pentylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting 5-bromo-4-(difluoromethyl)-N-(tert-pentyl)pyridin-2-amine (Intermediate 50) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₅F₂N₅O₃S, 523.6; m/z found, 524.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.04-8.00 (m, 1H), 7.64-7.55 (m, 1H), 7.00-6.62 (m, 2H), 4.77 (s, 1H), 4.27-4.19 (m, 1H), 3.60-3.32 (m, 4H), 2.96 (s, 1H), 2.90-2.87 (m, 1H), 2.25-2.14 (m, 1H), 1.92-1.79 (m, 3H), 1.65-1.50 (m, 1H), 1.39 (s, 6H), 1.31 (s, 6H), 1.22 (d, J=6.3 Hz, 2H), 1.02 (d, J=6.4 Hz, 1H), 0.91-0.86 (m, 3H).

Example 97 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-((2-cyclopropylpropan-2-yl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(2-cyclopropylpropan-2-yl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 48) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₇H₃₅F₂N₅O₃S, 547.7; m/z found, 548.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.03 (s, 1H), 7.64-7.57 (m, 1H), 6.91-6.61 (m, 2H), 5.02 (s, 1H), 4.73-4.65 (m, 1H), 4.25-4.18 (m, 1H), 3.48 (d, J=6.2 Hz, 2H), 2.09 (s, 1H), 1.81-1.72 (m, 2H), 1.60-1.51 (m, 2H), 1.48-1.39 (m, 4H), 1.33-1.30 (m, 12H), 1.29-1.24 (m, 1H), 0.53-0.45 (m, 2H), 0.45-0.39 (m, 2H).

Example 98 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-(tert-pentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(tert-pentyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 51) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.6; m/z found, 554.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.14 (s, 1H), 7.67-7.59 (m, 1H), 6.65 (s, 1H), 4.82 (s, 1H), 4.69 (s, 1H), 4.21 (s, 1H), 3.48 (d, J=6.3 Hz, 2H), 2.97-2.87 (m, 1H), 2.22 (s, 1H), 1.87-1.81 (m, 2H), 1.79-1.72 (m, 2H), 1.57-1.48 (m, 2H), 1.44-1.41 (m, 3H), 1.39 (s, 6H), 1.31 (s, 6H), 0.89-0.85 (m, 3H).

Example 99 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(4-(trifluoromethyl)-6-((1-(trifluoromethyl)cyclobutyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described for Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(trifluoromethyl)-N-(1-(trifluoromethyl)cyclobutyl)pyridin-2-amine (Intermediate 52) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₂₉F₆N₅O₃S, 605.6; m/z found, 606.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.22 (s, 1H), 7.63-7.55 (m, 1H), 6.64 (s, 1H), 5.33 (s, 1H), 4.72-4.32 (m, 2H), 3.49 (d, J=6.3 Hz, 2H), 2.70-2.40 (m, 4H), 2.14-2.01 (m, 3H), 1.82-1.64 (m, 4H), 1.49-1.42 (m, 4H), 1.32 (s, 6H).

Example 100 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(4-(trifluoromethyl)-6-((1-(trifluoromethyl)cyclobutyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(trifluoromethyl)-N-(1-(trifluoromethyl)cyclobutyl)pyridin-2-amine (Intermediate 52) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₂₇F₈N₅O₃S, 629.6; m/z found, 630.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.21 (s, 1H), 7.55-7.45 (m, 1H), 6.64 (s, 1H), 5.33-5.25 (m, 1H), 4.79-4.43 (m, 1H), 4.17-3.77 (m, 2H), 3.57-3.43 (m, 2H), 2.71-2.40 (m, 5H), 2.17-2.04 (m, 3H), 1.96-1.80 (m, 1H), 1.37 (d, J=6.4 Hz, 2H), 1.34-1.32 (m, 6H), 1.31-1.25 (m, 1H).

Example 101 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and (S)-5-bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 53) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₂₉F₆N₅O₃S, 593.6; m/z found, 594.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20 (s, 1H), 7.62-7.54 (m, 1H), 6.77 (s, 1H), 4.93-4.36 (m, 4H), 3.49 (d, J=6.3 Hz, 2H), 2.02-1.92 (m, 2H), 1.75 (br s, 2H), 1.67-1.59 (m, 3H), 1.49-1.41 (m, 4H), 1.32 (s, 6H), 1.07-1.01 (m, 3H).

Example 102 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and (S)-5-bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 53) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₂₇F₈N₅O₃S, 617.6; m/z found, 618.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20 (s, 1H), 7.54-7.45 (m, 1H), 6.76 (s, 1H), 4.92-4.43 (m, 3H), 4.14-3.81 (m, 2H), 3.57-3.42 (m, 2H), 2.62-2.47 (m, 1H), 2.14-1.92 (m, 2H), 1.90-1.77 (m, 1H), 1.68-1.58 (m, 1H), 1.36 (d, J=6.3 Hz, 2H), 1.33 (d, J=3.5 Hz, 6H), 1.29 (d, J=6.6 Hz, 1H), 1.08-1.02 (m, 3H).

Example 103 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-(tert-pentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(tert-pentyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 51) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₂F₅N₅O₃S, 577.6; m/z found, 578.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12 (s, 1H), 7.55-7.46 (m, 1H), 6.64 (s, 1H), 4.79 (s, 1H), 4.68-4.46 (m, 1H), 4.15-3.78 (m, 2H), 3.56-3.43 (m, 2H), 2.62-2.46 (m, 1H), 2.15-1.99 (m, 1H), 1.96-1.78 (m, 3H), 1.40 (d, J=2.3 Hz, 6H), 1.36 (d, J=6.4 Hz, 2H), 1.33 (d, J=2.5 Hz, 6H), 1.29 (d, J=6.5 Hz, 1H), 0.92-0.86 (m, 3H).

Example 104 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-((1-(trifluoromethyl)cyclobutyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-4-(trifluoromethyl)-N-(1-(trifluoromethyl)cyclobutyl)pyridin-2-amine (Intermediate 52) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₂₉F₆N₅O₃S, 593.6; m/z found, 594.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.24 (s, 1H), 7.61-7.52 (m, 1H), 6.63 (s, 1H), 5.33 (s, 1H), 4.40-4.11 (m, 1H), 3.59-3.43 (m, 4H), 2.70-2.61 (m, 2H), 2.50-2.40 (m, 2H), 2.11-2.04 (m, 3H), 2.01-1.92 (m, 2H), 1.80-1.72 (m, 1H), 1.59-1.51 (m, 1H), 1.33-1.30 (m, 6H), 1.24 (d, J=6.3 Hz, 2H), 1.12 (d, J=6.4 Hz, 1H).

Example 105 (S)-5-(6-((2-Cyclopropylpropan-2-yl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(2-cyclopropylpropan-2-yl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 48) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₅F₂N₅O₃S, 535.7; m/z found, 536.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.04-7.97 (m, 1H), 7.62-7.53 (m, 1H), 6.88-6.64 (m, 2H), 5.04 (s, 1H), 4.30-4.20 (m, 1H), 3.60-3.33 (m, 4H), 2.03-1.99 (m, 1H), 1.70-1.60 (m, 2H), 1.95-1.72 (m, 2H), 1.57-1.50 (m, 1H), 1.33-1.30 (m, 12H), 1.23 (d, J=6.3 Hz, 2H), 1.02 (d, J=6.4 Hz, 1H), 0.53-0.48 (m, 2H), 0.44-0.40 (m, 2H).

Example 106 (S)-5-(6-((2-Cyclopropylpropan-2-yl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(2-cyclopropylpropan-2-yl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 48) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₃F₄N₅O₃S, 571.6; m/z found, 572.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.01-7.96 (m, 1H), 7.57-7.49 (m, 1H), 6.81-6.56 (m, 2H), 5.06 (s, 1H), 4.69-4.48 (m, 1H), 4.09-3.80 (m, 2H), 3.55-3.50 (m, 1H), 3.48 (s, 4H), 3.47-3.41 (m, 1H), 2.61-2.49 (m, 1H), 2.06-1.99 (m, 1H), 1.36 (d, J=6.4 Hz, 2H), 1.32 (s, 9H), 1.22 (d, J=6.6 Hz, 1H), 1.17-1.13 (m, 1H), 0.53-0.48 (m, 2H), 0.44-0.40 (m, 2H).

Example 107 (S)-5-(6-((2-Cyclopropylpropan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(2-cyclopropylpropan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 45) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.6; m/z found, 590.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.13 (s, 1H), 7.55-7.47 (m, 1H), 6.80 (s, 1H), 5.10 (s, 1H), 4.70-4.45 (m, 1H), 4.14-3.78 (m, 2H), 3.56-3.43 (m, 2H), 2.60-2.47 (m, 1H), 2.18-2.00 (m, 1H), 1.94-1.79 (m, 1H), 1.36 (d, J=6.4 Hz, 2H), 1.34-1.31 (m, 12H), 1.30-1.25 (m, 2H), 0.54-0.47 (m, 2H), 0.44-0.38 (m, 2H).

Example 108 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)-5-(6-(tert-pentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(tert-pentyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 51) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₆F₃N₅O₃S, 555.7; m/z found, 556.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.23-8.14 (m, 1H), 7.68-7.59 (m, 1H), 6.66 (s, 1H), 4.95-4.44 (m, 2H), 3.95-3.34 (m, 3H), 2.96-2.77 (m, 1H), 2.27-2.16 (m, 1H), 1.88-1.81 (m, 2H), 1.66-1.47 (m, 4H), 1.39 (s, 6H), 1.31 (s, 6H), 1.18-1.09 (m, 3H), 0.89-0.84 (m, 3H).

Example 109 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)-5-(6-(tert-pentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-pentyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 51) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₃S, 541.6; m/z found, 542.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.17-8.14 (m, 1H), 7.65-7.52 (m, 1H), 6.64-6.61 (m, 1H), 4.79 (s, 1H), 4.27-4.17 (m, 1H), 3.60-3.36 (m, 4H), 2.13 (s, 1H), 2.08-2.02 (m, 1H), 1.91-1.72 (m, 4H), 1.56-1.48 (m, 1H), 1.41-1.38 (m, 6H), 1.31 (s, 6H), 1.23 (d, J=6.3 Hz, 2H), 1.10 (d, J=6.4 Hz, 1H), 0.90-0.86 (m, 3H).

Example 110 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and (S)-5-bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 44) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₃H₂₅F₈N₅O₃S, 603.5; m/z found, 604.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.17 (s, 1H), 7.57-7.48 (m, 1H), 6.73-6.65 (m, 1H), 5.58-5.32 (m, 1H), 5.02-4.91 (m, 1H), 4.49-3.80 (m, 3H), 3.58-3.43 (m, 2H), 2.66-2.49 (m, 1H), 2.21-2.04 (m, 2H), 1.40-1.36 (m, 5H), 1.33 (d, J=6.1 Hz, 6H), 1.29-1.26 (m, 1H).

Example 111 N-(2-Hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 53) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₂₉F₆N₅O₃S, 581.6; m/z found, 582.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.23-8.20 (m, 1H), 7.61-7.52 (m, 1H), 6.76-6.73 (m, 1H), 5.11-4.96 (m, 1H), 4.81 (s, 1H), 4.44-4.14 (m, 1H), 3.59-3.38 (m, 4H), 2.10-1.88 (m, 4H), 1.80-1.61 (m, 2H), 1.58-1.50 (m, 1H), 1.34-1.30 (m, 6H), 1.24 (d, J=6.3 Hz, 2H), 1.10 (d, J=6.4 Hz, 1H), 1.07-1.02 (m, 3H).

Example 112 N-(2-Hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and (S)-5-bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 53) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₁F₆N₅O₃S, 595.6; m/z found, 596.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.29-8.22 (m, 1H), 7.65-7.58 (m, 1H), 6.81 (s, 1H), 4.98-4.92 (m, 1H), 4.91-4.42 (m, 2H), 3.98-3.39 (m, 3H), 2.02-1.93 (m, 1H), 2.97-2.76 (m, 1H), 2.14-2.05 (m, 1H), 1.68-1.50 (m, 6H), 1.31 (s, 6H), 1.21-1.18 (m, 1H), 1.12-1.01 (m, 5H).

Example 113 (S)-5-(4-(Difluoromethyl)-6-(neopentylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-4-(difluoromethyl)-N-neopentylpyridin-2-amine (Intermediate 23) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₅F₂N₅O₃S, 523.2; m/z found, 524.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.03-7.97 (m, 1H), 7.64-7.53 (m, 1H), 6.99-6.65 (m, 2H), 5.05-4.95 (m, 1H), 4.32-4.17 (m, 1H), 3.60-3.35 (m, 4H), 3.19-3.12 (m, 2H), 2.31-2.17 (m, 1H), 2.06-1.88 (m, 2H), 1.78-1.72 (m, 1H), 1.65-1.50 (m, 1H), 1.31 (s, 6H), 1.22 (d, J=6.3 Hz, 2H), 1.02 (d, J=6.4 Hz, 1H), 1.01-0.98 (m, 9H).

Example 114 (S)-5-(4-(Difluoromethyl)-6-(neopentylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 66: Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(difluoromethyl)-N-neopentylpyridin-2-amine (Intermediate 23) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₇F₂N₅O₃S, 537.3; m/z found, 538.3 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.04 (s, 1H), 7.70-7.59 (m, 1H), 6.92-6.62 (m, 2H), 5.10-5.02 (m, 1H), 4.91-4.39 (m, 1H), 3.92-3.33 (m, 3H), 1.86 (s, 1H), 1.69-1.49 (m, 4H), 3.00-2.74 (m, 1H), 3.20-3.15 (m, 2H), 2.43-2.31 (m, 1H), 1.44-1.34 (m, 1H), 1.30 (s, 6H), 1.16 (d, J=6.8 Hz, 1H), 1.11 (d, J=7.0 Hz, 2H), 0.99 (s, 9H).

Example 115 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(neopentylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(difluoromethyl)-N-neopentylpyridin-2-amine (Intermediate 23) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₃F₄N₅O₃S, 559.2; m/z found, 560.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.03-7.96 (m, 1H), 7.57-7.47 (m, 1H), 6.89-6.57 (m, 2H), 5.03-4.95 (m, 1H), 4.69-4.46 (m, 1H), 4.11-3.81 (m, 2H), 3.56-3.42 (m, 2H), 3.16 (d, J=5.9 Hz, 2H), 2.61-2.49 (m, 1H), 2.18-1.96 (m, 2H), 1.36 (d, J=6.4 Hz, 2H), 1.34-1.31 (m, 6H), 1.22 (d, J=6.6 Hz, 1H), 1.00 (s, 9H).

Example 116 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(neopentylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(difluoromethyl)-N-neopentylpyridin-2-amine (Intermediate 23) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₅F₂N₅O₃S, 535.2; m/z found, 536.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.02 (s, 1H), 7.78-7.63 (m, 1H), 6.87-6.63 (m, 2H), 5.21-5.04 (m, 1H), 4.70-4.63 (m, 1H), 4.25-4.17 (m, 1H), 3.49-3.46 (m, 2H), 3.19-3.14 (m, 2H), 2.06 (d, J=14.3 Hz, 1H), 1.80-1.71 (m, 2H), 1.59-1.51 (m, 2H), 1.47-1.39 (m, 4H), 1.30 (s, 6H), 0.99 (s, 9H).

Example 117 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-(((1-(trifluoromethyl)cyclobutyl)methyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-4-(trifluoromethyl)-N-((1-(trifluoromethyl)cyclobutyl)methyl)pyridin-2-amine (Intermediate 54) of 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₁F₆N₅O₃S, 607.2; m/z found, 608.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.24-8.19 (m, 1H), 7.60-7.50 (m, 1H), 6.70-6.66 (m, 1H), 5.10-4.97 (m, 1H), 4.38-4.16 (m, 1H), 3.92-3.77 (m, 2H), 3.58-3.40 (m, 4H), 2.37-2.29 (m, 2H), 2.09-1.99 (m, 4H), 1.98-1.96 (m, 1H), 1.94-1.73 (m, 2H), 1.56-1.51 (m, 1H), 1.33-1.30 (m, 6H), 1.24 (d, J=6.3 Hz, 2H), 1.12 (d, J=6.4 Hz, 1H).

Example 118 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(4-(trifluoromethyl)-6-(((1-(trifluoromethyl)cyclobutyl)methyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(trifluoromethyl)-N-((1-(trifluoromethyl)cyclobutyl)methyl)pyridin-2-amine (Intermediate 54) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₂₉F₈N₅O₃S, 643.2; m/z found, 644.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19 (s, 1H), 7.54-7.46 (m, 1H), 6.70 (s, 1H), 5.06-4.99 (m, 1H), 4.78-4.44 (m, 1H), 4.15-3.78 (m, 4H), 3.56-3.44 (m, 2H), 2.61-2.49 (m, 1H), 2.38-2.30 (m, 2H), 2.12-1.96 (m, 5H), 1.90-1.76 (m, 1H), 1.37-1.29 (m, 9H).

Example 119 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(4-(trifluoromethyl)-6-(((1-(trifluoromethyl)cyclobutyl)methyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(trifluoromethyl)-N-((1-(trifluoromethyl)cyclobutyl)methyl)pyridin-2-amine (Intermediate 54) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₇H₃₁F₆N₅O₃S, 619.2; m/z found, 620.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19 (s, 1H), 7.63-7.56 (m, 1H), 6.69 (s, 1H), 5.21-5.13 (m, 1H), 4.71-4.64 (m, 1H), 4.43-4.35 (m, 1H), 3.84 (d, J=6.1 Hz, 2H), 3.48 (d, J=6.3 Hz, 2H), 2.36-2.27 (m, 2H), 2.10 (s, 1H), 2.08-1.95 (m, 4H), 1.76 (br s, 2H), 1.70-1.65 (m, 2H), 1.48-1.41 (m, 4H), 1.32 (s, 6H).

Example 120 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)-5-(6-((3,3,3-trifluoro-2,2-dimethylpropyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(3,3,3-trifluoro-2,2-dimethylpropyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 55) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₁F₆N₅O₃S, 595.2; m/z found, 596.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.17 (s, 1H), 7.61-7.51 (m, 1H), 6.68-6.63 (m, 1H), 5.29-5.11 (m, 1H), 4.42-4.14 (m, 1H), 3.71-3.41 (m, 6H), 2.08-1.73 (m, 4H), 1.59-1.50 (m, 1H), 1.33-1.30 (m, 6H), 1.25 (d, J=6.3 Hz, 2H), 1.20-1.17 (m, 6H), 1.12 (d, J=6.4 Hz, 1H).

Example 121 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-((3,3,3-trifluoro-2,2-dimethylpropyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(3,3,3-trifluoro-2,2-dimethylpropyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 55) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₂₉F₈N₅O₃S, 631.2; m/z found, 632.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.15 (s, 1H), 7.56-7.47 (m, 1H), 6.71-6.65 (m, 1H), 5.16-5.06 (m, 1H), 4.77-4.43 (m, 1H), 4.13-4.03 (m, 1H), 3.96-3.77 (m, 1H), 3.71-3.43 (m, 4H), 2.63-2.47 (m, 1H), 2.20-2.00 (m, 1H), 1.97-1.81 (m, 1H), 1.36 (d, J=6.4 Hz, 2H), 1.34-1.32 (m, 6H), 1.31-1.25 (m, 1H), 1.20 (s, 6H).

Example 122 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-((3,3,3-trifluoro-2,2-dimethylpropyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(3,3,3-trifluoro-2,2-dimethylpropyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 55) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₁F₆N₅O₃S, 607.2; m/z found, 608.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17 (s, 1H), 7.62-7.55 (m, 1H), 6.69 (s, 1H), 5.07 (t, J=6.5 Hz, 1H), 4.68 (s, 1H), 4.38 (s, 1H), 3.63 (d, J=6.4 Hz, 2H), 3.48 (d, J=6.3 Hz, 2H), 2.00 (s, 1H), 1.81-1.62 (m, 4H), 1.49-1.41 (m, 4H), 1.32 (s, 6H), 1.19 (s, 6H).

Example 123 (S)-5-(4-(Difluoromethyl)-6-((1-(trifluoromethyl)cyclobutyl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-4-(difluoromethyl)-N-(1-(trifluoromethyl)cyclobutyl)pyridin-2-amine (Intermediate 56) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.2; m/z found, 576.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.02 (m, 1H), 7.60-7.49 (m, 1H), 6.99-6.62 (m, 2H), 5.22 (s, 1H), 4.36-4.17 (m, 1H), 3.59-3.36 (m, 4H), 2.71-2.63 (m, 2H), 2.50-2.40 (m, 2H), 2.13-2.06 (m, 2H), 2.04-1.99 (m, 1H), 1.94-1.75 (m, 2H), 1.59-1.51 (m, 1H), 1.32 (s, 6H), 1.23 (d, J=6.3 Hz, 2H), 1.04 (d, J=6.4 Hz, 1H).

Example 124 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-((1-(trifluoromethyl)cyclobutyl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(difluoromethyl)-N-(1-(trifluoromethyl)cyclobutyl)pyridin-2-amine (Intermediate 56) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₂₈F₇N₅O₃S, 611.2; m/z found, 612.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.08-8.03 (m, 1H), 7.55-7.44 (m, 1H), 6.84-6.53 (m, 2H), 5.20 (s, 1H), 4.77-4.46 (m, 1H), 4.15-3.78 (m, 2H), 3.56-3.44 (m, 2H), 2.71-2.40 (m, 5H), 2.18-2.01 (m, 3H), 1.93-1.78 (m, 1H), 1.37 (d, J=6.4 Hz, 2H), 1.34-1.30 (m, 6H), 1.26-1.22 (m, 1H).

Example 125 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-(((1-(trifluoromethyl)cyclopropyl)methyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-4-(trifluoromethyl)-N-((1-(trifluoromethyl)cyclopropyl)methyl)pyridin-2-amine (Intermediate 57) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₂₉F₆N₅O₃S, 593.2; m/z found, 594.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17 (s, 1H), 7.62-7.51 (m, 1H), 6.67-6.63 (m, 1H), 5.31-5.17 (m, 1H), 4.40-4.14 (m, 1H), 3.75-3.41 (m, 6H), 2.08-1.73 (m, 4H), 1.59-1.50 (m, 1H), 1.32 (s, 6H), 1.24 (d, J=6.3 Hz, 2H), 1.12 (d, J=6.4 Hz, 1H), 1.07-1.01 (m, 2H), 0.90-0.84 (m, 2H).

Example 126 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(4-(trifluoromethyl)-6-(((1-(trifluoromethyl)cyclopropyl)methyl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-4-(trifluoromethyl)-N-((1-(trifluoromethyl)cyclopropyl)methyl)pyridin-2-amine (Intermediate 57) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₂₇F₈N₅O₃S, 629.2; m/z found, 630.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.14 (s, 1H), 7.54-7.45 (m, 1H), 6.68 (s, 1H), 5.23-5.12 (m, 1H), 4.78-4.42 (m, 1H), 4.14-3.79 (m, 2H), 3.75-3.62 (m, 2H), 3.57-3.43 (m, 2H), 2.62-2.47 (m, 1H), 2.21-2.01 (m, 1H), 1.95-1.79 (m, 1H), 1.36 (d, J=6.3 Hz, 2H), 1.34-1.31 (m, 6H), 1.30 (d, J=6.2 Hz, 1H), 1.08-1.04 (m, 2H), 0.91-0.85 (m, 2H).

Example 127 5-(6-((2,2-Difluorocyclopentyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(2,2-difluorocyclopentyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 64: Step B) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.2; m/z found, 576.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.21 (s, 1H), 7.61-7.50 (m, 1H), 6.76-6.71 (m, 1H), 5.21-5.10 (m, 1H), 4.67-4.44 (m, 1H), 4.39-4.15 (m, 1H), 3.57-3.39 (m, 4H), 2.39-2.29 (m, 1H), 2.27-2.13 (m, 2H), 2.12-1.96 (m, 2H), 1.94-1.75 (m, 4H), 1.66-1.60 (m, 1H), 1.57-1.49 (m, 1H), 1.32 (s, 6H), 1.26-1.23 (m, 2H), 1.15-1.09 (m, 1H).

Example 128 5-(6-(((S*)-1-Cyclopropylpropyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1-cyclopropylpropyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 24) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: CHIRALPAK AD-H 5 μm 250×20 mm, Mobile phase: 90% CO₂, 10% MeOH (0.3% iPrNH₂), second eluting peak) to separate diastereomers. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.2; m/z found, 554.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.13 (s, 1H), 7.65-7.51 (m, 1H), 6.60 (s, 1H), 4.96 (d, J=7.8 Hz, 1H), 4.33-4.15 (m, 1H), 3.67-3.33 (m, 5H), 3.32-3.18 (m, 1H), 2.14-1.48 (m, 5H), 1.38-1.21 (m, 9H), 1.12-1.07 (m, 1H), 1.06-0.81 (m, 4H), 0.64-0.52 (m, 1H), 0.50-0.42 (m, 1H), 0.37-0.25 (m, 2H).

Example 129 5-(6-(((R*)-1-Cyclopropylpropyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1-cyclopropylpropyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 24) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: CHIRALPAK AD-H 5 μm 250×20 mm, Mobile phase: 90% CO₂, 10% MeOH (0.3% iPrNH₂), first eluting peak) to separate diastereomers. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.2; m/z found, 554.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.14 (s, 1H), 7.63-7.52 (m, 1H), 6.60 (s, 1H), 4.90 (d, J 7.7 Hz, 1H), 4.34-4.14 (m, 1H), 3.67-3.18 (m, 5H), 3.32-3.18 (m, 1H), 2.13-1.48 (m, 5H), 1.37-1.17 (m, 9H), 1.13-0.79 (m, 5H), 0.62-0.41 (m, 2H), 0.38-0.24 (m, 2H).

Example 130 4-((s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S*)-1-cyclopropyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1-cyclopropylpropyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 24) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 31AC: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. A purification was performed via chiral SFC (Stationary phase: Chiralpak AS-H, 5 μm, 250×20 mm, Mobile phase: 0.5% isopropylamine, 75% CO₂, 25% MeOH, second eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₇H₃₄F₃N₅O₃S, 565.2; m/z found, 566.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12 (s, 1H), 7.61-7.57 (m, 1H), 6.61 (s, 1H), 4.90 (d, J=8.2 Hz, 1H), 4.68 (s, 1H), 4.30 (s, 1H), 3.48 (d, J=6.3 Hz, 2H), 3.29-3.22 (m, 1H), 1.95-1.52 (m, 5H), 1.46-1.38 (m, 4H), 1.32-1.18 (m, 7H), 1.11-0.84 (m, 5H), 0.62-0.51 (m, 1H), 0.51-0.42 (m, 1H), 0.37-0.23 (m, 2H).

Example 131 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((R*)-1-cyclopropyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1-cyclopropylpropyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 24) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. A purification was performed via chiral SFC (Stationary phase: Chiralpak AS-H, 5 μm, 250×20 mm, Mobile phase: 0.5% isopropylamine, 75% CO₂, 25% MeOH, first eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₇H₃₄F₃N₅O₃S, 565.2; m/z found, 566.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12 (s, 1H), 7.62-7.60 (m, 1H), 6.62 (s, 1H), 4.93 (d, J=8.2 Hz, 1H), 4.68 (s, 1H), 4.29 (s, 1H), 3.48 (d, J=6.3 Hz, 2H), 3.33-3.20 (m, 1H), 2.13-1.51 (m, 5H), 1.47-1.41 (m, 4H), 1.32-1.18 (m, 7H), 1.04-0.80 (m, 5H), 0.63-0.52 (m, 1H), 0.52-0.40 (m, 1H), 0.37-0.24 (m, 2H).

Example 132 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)-5-(6-((1,1,1-trifluoro-2-methylpropan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1,1,1-trifluoro-2-methylpropan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 58) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₂₉F₆N₅O₃S, 581.6; m/z found, 582.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.23-8.21 (m, 1H), 7.59-7.52 (m, 1H), 6.79 (s, 1H), 4.94-4.92 (m, 1H), 4.41-4.33 (m, 0.3H), 4.24-4.14 (m, 0.7H), 3.66-3.39 (m, 4H), 2.10-2.03 (m, 1H), 2.11-1.82 (m, 3H), 1.82-1.62 (m, 6H), 1.60-1.50 (m, 1H), 1.41-1.27 (m, 6H), 1.24 (d, J=6.3 Hz, 2.3H), 1.13 (d, J=6.4 Hz, 0.7H).

Example 133 (S)-5-(6-(tert-Butylamino)-4-(difluoromethyl)pyridin-3-yl)-N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 59) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 73: Step C) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.6; m/z found, 522.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.04-7.99 (m, 1H), 7.61-7.52 (m, 1H), 7.03-6.60 (m, 2H), 4.84 (s, 1H), 4.31-4.09 (m, 1.3H), 3.76-3.52 (m, 2.7H), 3.50-3.30 (m, 1H), 2.77-2.63 (m, 1H), 2.23-1.49 (m, 9H), 1.46 (s, 9H), 1.32-1.18 (m, 3H), 1.01 (d, J=6.4 Hz, 1H).

Example 134 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 41: Step B) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 73: Step C) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.17 (s, 1H), 7.63-7.54 (m, 1H), 6.63 (s, 1H), 4.90 (s, 1H), 4.30-4.15 (m, 1H), 3.74-3.50 (m, 2.5H), 3.49-3.34 (m, 1.5H), 2.90-2.75 (m, 1H), 2.21-1.48 (m, 10H), 1.45 (s, 9H), 1.23 (d, J=6.3 Hz, 2.3H), 1.09 (d, J=6.4 Hz, 0.7H).

Example 135 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₃H₂₆F₇N₅O₃S, 585.5; m/z found, 586.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.06 (d, J=13.1 Hz, 1H), 7.55-7.47 (m, 1H), 6.90-6.52 (m, 2H), 5.04-4.71 (m, 2.3H), 4.55-4.46 (m, 0.7H), 4.20-3.77 (m, 2H), 3.60-3.40 (m, 2H), 2.71-2.47 (m, 1H), 2.26-2.00 (m, 1H), 1.85 (d, J=35.4 Hz, 1H), 1.46-1.21 (m, 12H).

Example 136 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 562.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.07 (s, 1H), 7.62-7.56 (m, 1H), 6.76 (d, J=12.2 Hz, 2H), 5.02-4.86 (m, 2H), 4.68 (t, J=4.7 Hz, 1H), 4.37 (t, J=4.6 Hz, 1H), 3.49 (d, J=6.2 Hz, 2H), 2.02 (s, 1H), 1.83-1.60 (m, 4H), 1.53-1.38 (m, 7H), 1.32 (s, 6H).

Example 137 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-((dicyclopropylmethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methypropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(dicyclopropylmethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 25) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₈H₃₄F₃N₅O₃S, 577.7; m/z found, 578.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12 (s, 1H), 7.63-7.57 (m, 1H), 6.64 (s, 1H), 4.95 (d, J=8.0 Hz, 1H), 4.69 (s, 1H), 4.30 (s, 1H), 3.50-3.47 (m, 2H), 3.24 (q, J=7.5 Hz, 1H), 2.06-1.95 (m, 1H), 1.82-1.70 (m, 2H), 1.65-1.55 (m, 2H), 1.50-1.40 (m, 4H), 1.32 (s, 6H), 1.05-0.95 (m, 2H), 0.61-0.28 (m, 8H).

Example 138 (S)-5-(6-((Dicyclopropylmethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(dicyclopropylmethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 25) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₇H₃₂F₅N₅O₃S, 601.6; m/z found, 602.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10 (s, 1H), 7.49 (s, 1H), 6.64 (s, 1H), 4.96 (d, J=7.9 Hz, 1H), 4.72-4.64 (m, 0.3H), 4.52-4.45 (m, 0.7H), 4.20-3.79 (m, 2H), 3.56-3.44 (m, 2H), 3.23 (q, J=7.4 Hz, 1H), 2.65-2.45 (m, 1H), 2.23-1.98 (m, 1H), 1.90-1.80 (m, 1H), 1.43-1.21 (m, 9H), 1.05-0.95 (m, 2H), 0.61-0.28 (m, 8H).

Example 139 (S)-5-(6-((Dicyclopropylmethyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(dicyclopropylmethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 25) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₇H₃₄F₃N₅O₃S, 565.6; m/z found, 566.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.13 (d, J=1.7 Hz, 1H), 7.59-7.54 (m, 1H), 6.63 (s, 1H), 4.95 (d, J=8.1 Hz, 1H), 4.32-4.17 (m, 1H), 3.68-3.34 (m, 4H), 3.26-3.19 (m, 1H), 2.13-1.68 (m, 4H), 1.63-1.47 (s, 1H), 1.32 (s, 6H), 1.24 (d, J=6.3 Hz, 2H), 1.11 (d, J=6.4 Hz, 1H), 1.06-0.93 (m, 2H), 0.64-0.27 (m, 8H).

Example 140 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70: Step B) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₂F₃N₅O₃S, 551.6; m/z found, 552.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.16 (s, 1H), 7.62-7.55 (m, 1H), 6.51 (s, 1H), 5.20 (s, 1H), 4.69 (s, 1H), 4.31 (s, 1H), 3.48 (d, J=6.3 Hz, 2H), 2.30-2.24 (m, 2H), 2.16-2.14 (m, 2H), 2.07-1.88 (m, 3H), 1.76 (s, 2H), 1.65-1.57 (m, 2H), 1.54 (s, 3H), 1.49-1.41 (m, 4H), 1.32 (s, 6H).

Example 141 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.14 (s, 1H), 7.54-7.48 (m, 1H), 6.51 (s, 1H), 5.24 (s, 1H), 4.69-4.66 (m, 0.3H), 4.51-4.47 (m, 0.7H), 4.12-4.01 (m, 1H), 3.95-3.76 (m, 1H), 3.58-3.41 (m, 2H), 2.63-2.47 (m, 1H), 2.31-2.25 (m, 2H), 2.20-1.84 (m, 6H), 1.55 (s, 3H), 1.40-1.23 (m, 9H).

Example 142 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(trifluormethyl)pyridin-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-N-(1-cyclopropylethyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 18) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.12 (s, 1H), 7.53-7.49 (m, 1H), 6.61 (s, 1H), 5.03 (d, J=7.4 Hz, 1H), 4.75-4.65 (m, 0.2H) 4.51-4.46 (m, 0.8H), 4.16-4.00 (m, 1H), 3.93-3.80 (m, 1H), 3.57-3.33 (m, 3H), 2.65-2.46 (m, 1H), 2.23-1.81 (m, 2H), 1.37-1.28 (m, 12H), 1.00-0.92 (m, 1H), 0.62-0.44 (m, 2H), 0.41-0.24 (m, 2H).

Example 143 (S)-5-(6-(tert-Butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 59) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₄H₃₁F₄N₅O₃S, 545.6; m/z found, 546.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.02-7.99 (m, 1H), 7.52-7.48 (m, 1H), 6.90-6.34 (m, 2H), 4.85 (s, 1H), 4.72-4.61 (m, 0.3H), 4.58-4.46 (m, 0.7H), 4.09-4.00 (m, 1H), 3.92-3.85 (m, 1H), 3.55-3.43 (m, 2H), 2.60-2.53 (m, 1H), 2.15-2.05 (m, 1H), 1.90-1.82 (m, 1H), 1.46-1.44 (m, 10.5H), 1.41-1.17 (m, 7.5H).

Example 144 5-(4-Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 1AB, Step D) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S, 563.6; m/z found, 564.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10 (s, 1H), 7.63-7.56 (m, 1H), 6.96-6.62 (m, 2H), 5.03-4.83 (m, 2.5H), 4.43 (d, J=12.8 Hz, 0.5H), 3.95-3.87 (m, 0.5H), 3.50-3.46 (m, 2H), 3.38 (d, J=13.5 Hz, 0.5H), 3.06-2.90 (m, 0.5H), 2.82-2.77 (m, 0.5H), 2.14-1.97 (m, 1H), 1.73-1.49 (m, 3H), 1.45-1.41 (m, 4H), 1.31 (s, 7H), 1.20-1.10 (m, 4H).

Example 145 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₃H₂₈F₅N₅O₃S, 549.6; m/z found, 550.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09 (s, 0.7H), 8.04 (s, 0.3H), 7.60-7.50 (m, 1H), 7.06-6.60 (m, 2H), 5.02-4.79 (m, 2H), 4.39-4.36 (m, 0.3H), 4.26-4.15 (m, 0.7H), 3.65-3.35 (m, 4H), 2.13-1.48 (m, 5H), 1.42 (d, J=6.8 Hz, 3H), 1.32 (s, 6H), 1.23 (d, J=6.3 Hz, 2H), 1.04 (d, J=6.4 Hz, 1H).

Example 146 (S)-5-(5-Cyano-6-(cyclohexylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-2-(cyclohexylamino)nicotinonitrile (Intermediate 9) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI) mass calcd for C₂₆H₃₄N₆O₃S 510.2 m/z: found 511.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.43 (d, J=2.5 Hz, 1H), 7.92-7.88 (m, 1H), 7.63-7.54 (m, 1H), 5.29-5.23 (m, 1H), 4.39-3.96 (m, 2H), 3.72-3.21 (m, 4H), 2.39-2.30 (m, 1H), 2.12-2.06 (m, 1H), 2.03-1.98 (m, 1H), 1.94-1.86 (m, 1H), 1.82-1.75 (m, 3H), 1.70-1.65 (m, 1H), 1.64-1.57 (m, 1H), 1.47-1.38 (m, 2H), 1.35 (d, J=6.4 Hz, 2H), 1.31-1.29 (m, 6H), 1.28-1.25 (m, 2H), 0.93 (d, J=6.4 Hz, 1H).

Example 147 (S)—N-(2-Hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-((1-(trifluoromethyl)cyclopropyl)amino)pyridin-3-yl)thiazole-2-carboxamide

An oven-dried vial under N₂ was charged with (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (62 mg, 0.18 mmol, Intermediate 69), 5-bromo-4-(trifluoromethyl)-N-(1-(trifluoromethyl)cyclopropyl)pyridin-2-amine (84 mg, 0.18 mmol, Intermediate 63: Step B) K₂CO₃ (100 mg, 0.72 mmol), pivalic acid (7 mg, 0.07 mmol), di-(1-adamantyl)-n-butylphosphine (20 mg, 0.05 mmol) and Pd₂(dba)₃ (25 mg, 0.030 mmol). The vial was evacuated and backfilled with N₂ two times, then butyronitrile (1.1 mL, sparged with N₂ for 1 hour prior to addition) was added and the reaction was stirred at 100° C. for 22 hours. The reaction was cooled to rt, filtered through Celite*, rinsing with EtOAc, and concentrated to dryness. The residue was re-subjected to the reaction conditions, by adding K₂CO₃ (100 mg, 0.72 mmol), pivalic acid (7.4 mg, 0.07 mmol), di-(1-adamantyl)-n-butylphosphine (20.4 mg, 0.05 mmol) and Pd₂(dba)₃ (25 mg, 0.03 mmol). The vial was evacuated and backfilled with N₂, then butyronitrile (1.1 mL, sparged with N₂ for 1 hour prior to addition) was added and the mixture stirred at 100° C. for 18 hours. The reaction was allowed to cool to rt, then quenched with water (15 mL) and extracted with EtOAc (15 mL). The aqueous layer was further extracted with EtOAc (20 mL), then the organics were combined, washed with brine, dried over anhydrous sodium sulfate and concentrated to dryness. The residue was purified by FCC (0-10% MeOH/DCM) followed by basic HPLC to provide the title compound as a light yellow oil. MS (ESI): mass calcd. for C₂₄H₂₇F₆N₅O₃S, 579.6; m/z found, 580.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.26-8.23 (m, 1H), 7.60-7.50 (m, 1H), 7.43-7.34 (m, 1H), 6.99 (s, 1H), 6.99-6.94 (m, 1H), 5.71 (s, 1H), 4.42-4.15 (m, 1H), 3.59-3.45 (m, 3H), 2.09-2.02 (m, 1H), 1.96-1.92 (m, 1H), 1.80-1.73 (m, 1H), 1.58-1.54 (m, 1H), 1.33-1.31 (m, 6H), 1.24 (d, J=6.3 Hz, 2H), 1.19-1.16 (m, 2H), 1.13 (d, J=6.5 Hz, 1H), 0.86-0.82 (m, 2H).

Example 148 5-(6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl)-N-((1R)-2-hydroxy-1-methyl-ethyl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

To a microwave vial under N₂ was added ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (131 mg, 0.28 mmol, Intermediate 106), (R)-(−)-2-amino-1-propanol (105 mg, 1.4 mmol) and EtOH (1.33 mL), and the reaction was stirred at 100° C. for 18 h. The reaction mixture was cooled to rt and partitioned between EtOAc (20 mL) and saturated aqueous NH₄Cl (20 mL). The layers were separated and the aqueous further extracted with EtOAc (2×15 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-100% EtOAc/Hexanes) to provide the title compound as a yellow oil. MS (ESI): mass calcd. for C₂₃H₃₁F₂N₅O₃S, 495.6; m/z found, 496.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.05-7.98 (m, 1H), 7.37-7.29 (m, 1H), 6.99-6.61 (m, 2H), 4.92-4.84 (s, 1H), 4.29-4.17 (m, 2H), 3.82-3.29 (m, 4H), 1.47-1.43 (m, 9H), 2.72-2.59 (s, 1H), 1.96-1.71 (m, 3H), 1.64-1.49 (m, 1H), 1.34-1.31 (d, J=6.8 Hz, 3H), 1.24-1.20 (d, J=6.3 Hz, 2H), 1.03-0.99 (d, J=6.4 Hz, 1H).

Example 149 [5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-2-(3-hydroxy-3-methyl-azetidine-1-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

To a microwave vial under N₂ was added ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (131 mg, 0.28 mmol, Intermediate 106), 3-hydroxy-3-methylazetidine HCl (183 mg, 1.4 mmol), DIPEA (0.27 mL, 1.54 mmol) and EtOH (1.33 mL), and the reaction was stirred at 100° C. for 15 h. The reaction mixture was cooled to rt and partitioned between EtOAc (20 mL) and saturated aqueous NH₄Cl (20 mL). The layers were separated and the aqueous further extracted with EtOAc (2×15 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-100% EtOAc/Hexanes) to provide the title compound as a yellow oil. MS (ESI): mass calcd. for C₂₄H₃₁F₂N₅O₃S, 507.6; m/z found, 508.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.02-7.93 (m, 1H), 6.95-6.58 (m, 2H), 4.92-4.86 (s, 1H), 4.63-4.49 (m, 2H), 4.43-4.16 (m, 1H), 4.16-4.09 (m, 3H), 3.60-3.22 (m, 3H), 2.09-2.03 (m, 2H), 1.97-1.72 (m, 3H), 1.55-1.49 (m, 1H), 1.47-1.41 (s, 9H), 1.24-1.18 (m, 2H), 1.01-0.90 (m, 1H).

Example 150 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-((3R,4S)-4-hydroxytetrahydrofuran-3-yl)-5-(4-(trifluoromethyl)-6-(((1S)-2,2,2-trifluoro-1-methyl-ethyl)amino)-3-pyridyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3S,4R)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 116) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₅F₆N₅O₄S, 593.5; m/z found, 594.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.21-8.16 (s, 1H), 7.35-7.28 (d, J=6.7 Hz, 1H), 6.74-6.67 (s, 1H), 5.39-5.32 (d, J=9.3 Hz, 1H), 5.02-4.92 (m, 1H), 4.72-4.63 (s, 1H), 4.49-4.27 (m, 3H), 4.25-4.14 (m, 2H), 3.87-3.74 (m, 2H), 3.31-3.26 (d, J=3.0 Hz, 1H), 1.80-1.69 (s, 2H), 1.68-1.53 (m, 2H), 1.51-1.42 (m, 4H), 1.42-1.38 (d, J=6.9 Hz, 3H).

Example 151 4-(1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1S,3S)-3-hydroxycyclopentyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1S,3S)-3-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₀F₅N₅O₃S, 587.6; m/z found, 588.1 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.11-8.06 (s, 1H), 7.18-7.11 (d, J=7.8 Hz, 1H), 6.92-6.61 (m, 2H), 4.88-4.58 (m, 4H), 4.53-4.46 (m, 1H), 4.15-4.08 (m, 1H), 2.42-2.06 (m, 3H), 2.02-1.94 (m, 1H), 1.87-1.78 (m, 1H), 1.76-1.70 (m, 2H), 1.69-1.66 (s, 2H), 1.65-1.56 (m, 2H), 1.51-1.38 (m, 6H), 1.07-1.00 (m, 3H).

Example 152 4-(1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1R,3R)-3-hydroxycyclopentyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,3R)-3-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₀F₅N₅O₃S, 587.6; m/z found, 588.1 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.11-8.06 (s, 1H), 7.20-7.14 (d, J=7.8 Hz, 1H), 6.92-6.61 (m, 2H), 4.96-4.59 (m, 4H), 4.53-4.45 (m, 1H), 4.13-4.09 (m, 1H), 2.42-2.06 (m, 3H), 2.01-1.92 (m, 1H), 1.85-1.77 (m, 2H), 1.76-1.71 (m, 3H), 1.65-1.55 (m, 2H), 1.51-1.38 (m, 6H), 1.07-1.00 (m, 3H).

Example 153 4-(1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-tetrahydropyran-4-yl-thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 4-aminotetrahydropyran for (R)-(−)-2-amino-1-propanol and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₀F₅N₅O₃S, 587.6; m/z found, 588.1 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.10-8.07 (s, 1H), 7.16-7.09 (d, J=8.3 Hz, 1H), 6.94-6.62 (m, 2H), 4.93-4.65 (m, 3H), 4.24-4.13 (m, 2H), 4.06-3.98 (m, 2H), 3.59-3.49 (m, 2H), 2.04-1.94 (m, 3H), 1.72-1.56 (m, 5H), 1.53-1.39 (m, 6H), 1.07-1.00 (m, 3H).

Example 154 4-(1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-(1,1-dioxothian-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 4-aminotetrahydro-2H-thiopyran 1,1-dioxide for (R)-(−)-2-amino-1-propanol and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₀F₅N₅O₄S₂, 635.7; m/z found, 636.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.11-8.06 (s, 1H), 7.68-7.54 (d, J=8.0 Hz, 1H), 6.91-6.60 (m, 2H), 4.86-4.61 (m, 2H), 4.32-4.18 (m, 1H), 4.08-3.99 (s, 1H), 1.57-1.54 (m, 3H), 3.22-3.12 (m, 4H), 2.48-2.25 (m, 4H), 2.00-1.94 (m, 1H), 1.66-1.59 (m, 1H), 1.49-1.36 (m, 6H), 1.06-1.00 (m, 3H).

Example 155 4-(1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-((3R,4S)-4-hydroxytetrahydrofuran-3-yl)-5-(4-(trifluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3S,4R)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-((1R,4R)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 100) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₇F₆N₅O₄S, 607.6; m/z found, 608.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.22-8.17 (s, 1H), 7.39-7.32 (d, J=6.7 Hz, 1H), 6.81-6.76 (s, 1H), 5.16-5.09 (d, J=9.8 Hz, 1H), 4.87-4.63 (m, 2H), 4.46-4.35 (m, 2H), 4.24-4.13 (m, 3H), 3.87-3.74 (m, 2H), 3.40-3.34 (s, 1H), 2.02-1.91 (m, 1H), 1.78-1.54 (m, 4H), 1.50-1.38 (m, 5H), 1.07-0.99 (m, 3H).

Example 156 4-(1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-((3S,4R)-4-hydroxytetrahydrofuran-3-yl)-5-(4-(trifluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3R,4S)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 100) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₇F₆N₅O₄S, 607.6; m/z found, 608.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.22-8.17 (s, 1H), 7.40-7.33 (d, J=6.7 Hz, 1H), 6.80-6.76 (s, 1H), 5.15-5.07 (d, J=9.7 Hz, 1H), 4.88-4.62 (m, 2H), 4.48-4.35 (m, 2H), 4.25-4.12 (m, 3H), 3.87-3.73 (m, 2H), 3.36-3.29 (s, 1H), 2.01-1.90 (m, 1H), 1.80-1.67 (m, 2H), 1.65-1.49 (m, 3H), 1.48-1.40 (m, 4H), 1.06-0.99 (m, 3H).

Example 157 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1R*,2R*)-2-hydroxycyclopropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

To a 25 mL round-bottom flask under N₂ was added N-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (377 mg, 0.55 mmol, Intermediate 101: Step D) and dry THF (3.1 mL). To this solution was added AcOH (47.4 μL, 0.83 mmol) followed by TBAF (0.83 mL, 0.83 mmol) and the resulting solution stirred at rt for 3 hours. The mixture was partitioned between brine (15 mL) and EtOAc (25 mL), and the organic phase was dried over anhydrous sodium sulfate, filtered and concentrated to dryness. The crude residue was purified by FCC 0-100% EtOAc/Hexanes) to provide a mixture of trans cyclopropyl isomers as a yellow oil. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak IC, 5 μm, 250×20 mm, Mobile phase: 20% EtOH+0.3% iPrNH₂, 80% CO₂, second eluting enantiomer). MS (ESI): mass calcd. for C₂₂H₂₄F₅N₅O₃S, 533.5; m/z found, 534.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.01 (m, 1H), 7.21-7.10 (m, 1H), 7.01-6.59 (m, 2H), 4.98-4.88 (m, 2H), 4.29-4.15 (m, 1H), 3.65-3.31 (m, 3H), 2.93-2.86 (m, 1H), 2.09-1.99 (m, 1H), 1.95-1.71 (m, 2H), 1.58-1.49 (m, 1H), 1.43-1.38 (d, J=6.3 Hz, 3H), 1.30-1.23 (m, 2H), 1.22-1.19 (d, J=6.3 Hz, 2H), 1.02-0.96 (m, 2H).

Example 158 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclopropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 157. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak IC, 5 μm, 250×20 mm, Mobile phase: 20% EtOH+0.3% iPrNH₂, 80% CO₂, first eluting enantiomer). MS (ESI): mass calcd. for C₂₂H₂₄F₅N₅O₃S, 533.5; m/z found, 534.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.02 (m, 1H), 7.19-7.08 (m, 1H), 7.03-6.60 (m, 2H), 4.99-4.83 (m, 2H), 4.33-4.15 (m, 1H), 3.64-3.30 (m, 3H), 2.94-2.87 (m, 1H), 2.08-2.01 (m, 1H), 1.95-1.72 (m, 3H), 1.58-1.49 (m, 1H), 1.44-1.39 (d, J=6.7 Hz, 3H), 1.28-1.24 (m, 1H), 1.23-1.21 (m, 2H), 1.02-0.96 (m, 2H).

Example 159 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((3R*,4R*)-4-hydroxytetrahydrofuran-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-4-aminotetrahydro-3-furanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 15% EtOH+0.3% iPrNH₂, 85% CO₂, second eluting enantiomer). MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₄S, 563.5; m/z found, 564.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.80-7.72 (m, 1H), 6.99-6.56 (m, 2H), 5.08-4.88 (m, 2H), 4.63-4.42 (m, 2H), 4.40-4.14 (m, 2H), 4.09-4.02 (dd, J=10.2, 4.5 Hz, 1H), 3.90-3.84 (m, 1H), 3.76-3.69 (m, 1H), 3.60-3.33 (m, 2H), 2.09-1.72 (m, 4H), 1.60-1.49 (m, 1H), 1.44-1.38 (d, J=6.8 Hz, 3H), 1.25-1.21 (d, J=6.3 Hz, 2H), 1.05-1.01 (d, J=6.4 Hz, 1H).

Example 160 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((3S*,4S*)-4-hydroxytetrahydrofuran-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 159. The pure diastereomer was isolated via SFC (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 15% EtOH+0.3% iPrNH₂, 85% CO₂, first eluting enantiomer). MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₄S, 563.5; m/z found, 564.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.01 (m, 1H), 7.77-7.69 (d, J=7.9 Hz, 1H), 7.00-6.61 (m, 2H), 5.00-4.81 (m, 2H), 4.64-4.55 (m, 1H), 4.52-4.46 (m, 1H), 4.37-4.15 (m, 2H), 4.10-4.04 (dd, J=10.3, 4.5 Hz, 1H), 3.90-3.85 (m, 1H), 3.76-3.70 (m, 1H), 3.60-3.38 (m, 2H), 2.09-1.74 (m, 4H), 1.58-1.52 (m, 1H), 1.43-1.40 (d, J=6.8 Hz, 3H), 1.24-1.20 (d, J=6.3 Hz, 2H), 1.09-1.05 (d, J=6.4 Hz, 1H).

Example 161 5-(6-((1-Cyclobutylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(1-cyclobutylethyl)-4-(trifluoromethyl)pyridine-2-amine (Intermediate 89) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.13 (s, 1H), 7.52-7.46 (m, 1H), 6.62 (s, 1H), 4.73 (d, J=8.3 Hz, 1.3H), 4.50-4.47 (m, 0.7H), 4.16-4.00 (m, 1H), 3.96-3.77 (m, 2H), 3.57-3.41 (m, 2H), 2.61-2.48 (m, 1H), 2.40-2.34 (m, 1H), 2.16-1.98 (m, 3H), 1.94-1.74 (m, 5H), 1.41-1.23 (m, 9H), 1.13 (dd, J=6.3, 2.3 Hz, 3H).

Example 162 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((3R*,4R*)-4-hydroxytetrahydrofuran-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-4-aminotetrahydro-3-furanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 15% EtOH+0.3% iPrNH₂, 85% CO₂, second eluting enantiomer). MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₄S, 577.6; m/z found, 578.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.08-7.99 (m, 1H), 7.82-7.74 (m, 1H), 7.01-6.59 (m, 2H), 5.03-4.95 (d, J=9.8 Hz, 1H), 4.85-4.68 (s, 1H), 4.62-4.41 (m, 2H), 4.39-3.83 (m, 4H), 3.75-3.70 (m, 1H), 3.58-3.32 (m, 2H), 2.09-2.01 (m, 1H), 1.99-1.87 (m, 2H), 1.80-1.72 (m, 1H), 1.66-1.50 (m, 2H), 1.23-1.20 (d, J=6.3 Hz, 2H), 1.08-0.99 (m, 4H).

Example 163 4-((s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S*)-1-cyclopropyl)amino)-4-(difluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(1-cyclopropylpropyl)-4-difluoromethyl)pyridine-2-amine (Intermediate 90) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 0.3% iPrNH₂, 75% CO₂, 25% EtOH/iPrOH (50/50), second eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₇H₃₅F₂N₅O₃S, 547.2; m/z found, 548.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.00 (s, 1H), 7.61-7.57 (m, 1H), 6.91-6.61 (m, 2H), 4.84 (d, J=8.2 Hz, 1H), 4.72-4.66 (m, 1H), 4.27-4.23 (m, 1H), 3.48 (d, J=6.3 Hz, 2H), 3.30-3.23 (m, 1H), 1.87-1.37 (m, 10H), 1.32-1.26 (m, 7H), 1.06-0.83 (m, 4H), 0.61-0.51 (m, 1H), 0.51-0.40 (m, 1H), 0.37-0.24 (m, 2H).

Example 164 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((R*)-1-cyclopropyl)amino)-4-(difluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(1-cyclopropylpropyl)-4-difluoromethyl)pyridine-2-amine (Intermediate 90) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 0.3% iPrNH₂, 75% CO₂, 25% EtOH/iPrOH (50/50), first eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₇H₃₅F₂N₅O₃S, 547.2; m/z found, 548.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.00 (s, 1H), 7.61-7.57 (m, 1H), 6.91-6.61 (m, 2H), 4.84 (d, J=8.2 Hz, 1H), 4.72-4.66 (m, 1H), 4.27-4.23 (m, 1H), 3.48 (d, J=6.3 Hz, 2H), 3.30-3.23 (m, 1H), 1.87-1.37 (m, 10H), 1.32-1.26 (m, 7H), 1.06-0.83 (m, 4H), 0.61-0.51 (m, 1H), 0.51-0.40 (m, 1H), 0.37-0.24 (m, 2H).

Example 165 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((3S*,4S*)-4-hydroxytetrahydrofuran-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 162. The pure diastereomer was isolated via SFC (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 15% EtOH+0.3% iPrNH₂, 85% CO₂, first eluting enantiomer). MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₄S, 577.6; m/z found, 578.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.08-7.99 (m, 1H), 7.83-7.76 (d, J=7.9 Hz, 1H), 6.98-6.60 (m, 2H), 5.03-4.96 (d, J=9.7 Hz, 1H), 4.84-4.70 (s, 1H), 4.61-4.42 (m, 2H), 4.28-4.13 (m, 2H), 4.08-4.02 (m, 1H), 3.89-3.83 (m, 1H), 3.74-3.70 (m, 1H), 3.58-3.38 (m, 2H), 2.10-1.49 (m, 7H), 1.21-1.17 (d, J=6.3 Hz, 2H), 1.08-1.01 (m, 4H).

Example 166 5-(6-(((S*)-1-Cyclopropyl)amino)-4-(difluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1-cyclopropylpropyl)-4-difluoromethyl)pyridine-2-amine (Intermediate 90) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 0.3% iPrNH₂, 82% CO₂, 18% iPrOH, second eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₇H₃₅F₂N₅O₃S, 535.2; m/z found, 536.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.00-7.96 (m, 1H), 7.59-7.52 (m, 1H), 7.04-6.56 (m, 2H), 4.85 (d, J=8.2 Hz, 1H), 4.34-4.17 (m, 1H), 3.65-3.18 (m, 4H), 2.12-1.45 (m, 7H), 1.40-1.18 (m, 9H), 1.07-0.83 (m, 5H), 0.62-0.40 (m, 2H), 0.38-0.23 (m, 2H).

Example 167 5-(6-(((R*)-1-Cyclopropyl)amino)-4-(difluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1-cyclopropylpropyl)-4-difluoromethyl)pyridine-2-amine (Intermediate 90) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 0.3% iPrNH₂, 82% CO₂, 18% iPrOH, first eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₇H₃₅F₂N₅O₃S, 535.2; m/z found, 536.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.02-7.96 (m, 1H), 7.64-7.50 (m, 1H), 7.03-6.58 (m, 2H), 4.87 (d, J=8.2 Hz, 1H), 4.35-4.16 (m, 1H), 3.65-3.18 (m, 4H), 2.16-1.49 (m, 7H), 1.40-1.16 (m, 9H), 1.07-0.80 (m, 5H), 0.61-0.52 (m, 1H), 0.52-0.42 (m, 1H), 0.38-0.24 (m, 2H).

Example 168 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(1-methylcyclobutyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 91) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₁F₄N₅O₃S, 557.2; m/z found, 558.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.02-7.98 (m, 1H), 7.55-7.45 (m, 1H), 6.90-6.50 (m, 2H), 5.18 (s, 1H), 4.70-4.49 (m, 1H), 4.17-3.98 (m, 1H), 3.95-3.77 (m, 1H), 3.61-3.38 (m, 2H), 2.66-2.45 (m, 1H), 2.34-2.21 (m, 2H), 2.21-2.02 (m, 3H), 2.01-1.83 (m, 3H), 1.55 (s, 3H), 1.41-1.16 (m, 9H).

Example 169 4-((1s,4s)-7-Azabicyclo[2.2[1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl))thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(1-methylcyclobutyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 91) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₃S, 533.2; m/z found, 534.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.04-8.02 (m, 1H), 7.62-7.59 (m, 1H), 6.90-6.52 (m, 1H), 5.17 (s, 1H), 4.71-4.66 (m, 1H), 4.27-4.23 (m, 1H), 3.48 (d, J=6.3 Hz, 1H), 2.97-2.88 (m, 2H), 2.33-2.08 (m, 4H), 2.01-1.86 (m, 2H), 1.54 (s, 5H), 1.48-1.42 (m, 3H), 1.33-1.26 (m, 9H), 0.96-0.78 (m, 1H).

Example 170 N-((3R,4S)-4-Hydroxytetrahydrofuran-3-yl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 4-((S)-2-methylpyrrolidine-1-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 103) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (3S,4R)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₄H₂₇F₆N₅O₄S, 595.6; m/z found, 596.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.23-8.17 (s, 1H), 7.39-7.28 (m, 1H), 6.76-6.71 (m, 1H), 5.28-5.12 (m, 1H), 4.88-4.74 (m, 1H), 4.48-4.35 (m, 2H), 4.27-4.14 (m, 3H), 3.90-3.73 (m, 2H), 3.60-3.31 (m, 3H), 2.12-2.05 (m, 1H), 1.98-1.88 (m, 2H), 1.79-1.50 (m, 3H), 1.26-1.22 (d, J=6.3 Hz, 3H), 1.07-1.01 (m, 3H).

Example 171 4-((1s,4s)-7-Azabicyclo[2.2[1]heptane-7-carbonyl)-5-(6-(((S*)-1-cyclobutylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(1-cyclobutylethyl)-4-(trifluoromethyl)pyridine-2-amine (Intermediate 89) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: Chiralpak IC, 5 μm, 250×20 mm, Mobile phase: 0.5% iPrNH₂, 85% CO₂, 15% MeOH, second eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₇H₃₄F₃N₅O₃S, 565.2; m/z found, 566.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.14 (s, 1H), 7.64-7.60 (m, 1H), 6.62 (s, 1H), 4.82 (d, J=8.3 Hz, 1H), 4.68 (s, 1H), 4.32 (s, 1H), 3.89-3.81 (m, 1H), 3.48 (d, J=6.2 Hz, 2H), 2.62-2.29 (m, 3H), 2.10-1.97 (m, 2H), 1.94-1.70 (m, 5H), 1.48-1.41 (m, 4H), 1.32 (s, 6H), 1.25 (s, 1H), 1.20-1.15 (m, 1H), 1.12 (d, J=6.4 Hz, 3H).

Example 172 4-((1s,4s)-7-Azabicyclo[2.2[1]heptane-7-carbonyl)-5-(6-(((R*)-1-cyclobutylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(1-cyclobutylethyl)-4-(trifluoromethyl)pyridine-2-amine (Intermediate 89) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: Chiralpak IC, 5 μm, 250×20 mm, Mobile phase: 0.5% iPrNH₂, 85% CO₂, 15% MeOH, first eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₇H₃₄F₃N₅O₃S, 565.2; m/z found, 566.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.14 (s, 1H), 7.64-7.60 (m, 1H), 6.62 (s, 1H), 4.82 (d, J=8.3 Hz, 1H), 4.68 (s, 1H), 4.33 (s, 1H), 3.89-3.81 (m, 1H), 3.48 (d, J=6.3 Hz, 2H), 2.59 (s, 2H), 2.43-2.31 (m, 1H), 2.07-2.00 (m, 2H), 1.96-1.69 (m, 5H), 1.48-1.40 (m, 4H), 1.32 (s, 6H), 1.25 (s, 1H), 1.20-1.16 (m, 1H), 1.12 (d, J=6.4 Hz, 3H).

Example 173 (S)-5-(4-difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1-methylcyclobutyl)-4-(difluoromethyl)pyridine-2-amine (Intermediate 91) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.2; m/z found, 522.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.03-7.99 (m, 1H), 7.61-7.53 (m, 1H), 7.01-6.50 (m, 2H), 5.20 (s, 1H), 4.36-4.17 (m, 1H), 3.64-3.30 (m, 4H), 2.35-1.83 (m, 10H), 1.83-1.49 (m, 4H), 1.31 (s, 6H), 1.28-1.20 (m, 2H), 1.02 (d, J=6.4 Hz, 1H).

Example 174 N-((3S,4R)-4-Hydroxytetrahydrofuran-3-yl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)-5-(4-(trifluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 4-((S)-2-methylpyrrolidine-1-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 103) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (3R,4S)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₄H₂₇F₆N₅O₄S, 595.6; m/z found, 596.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.22-8.16 (s, 1H), 6.79-6.75 (m, 1H), 4.87-4.76 (m, 1H), 4.41-4.31 (m, 2H), 4.26-4.14 (m, 3H), 3.91-3.84 (m, 1H), 3.77-3.72 (m, 1H), 3.60-3.31 (m, 2H), 2.13-2.06 (m, 1H), 1.98-1.87 (m, 2H), 1.79-1.70 (m, 1H), 1.64-1.50 (m, 2H), 1.26-1.23 (m, 3H), 1.09-0.99 (m, 4H).

Example 175 5-(6-(((S*)-1-Cyclobutylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1-cyclobutylethyl)-4-(trifluoromethyl)pyridine-2-amine (Intermediate 89) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: Chiralpak IC, 5 μm, 250×20 mm, Mobile phase: 0.5% iPrNH₂, 85% CO₂, 15% MeOH/iPrOH (50/50), second eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.2; m/z found, 554.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.16 (d, J=2.4 Hz, 1H), 7.63-7.50 (m, 1H), 6.61 (s, 1H), 4.76 (d, J=8.3 Hz, 1H), 4.33-4.17 (m, 1H), 3.87-3.77 (m, 1H), 3.61-3.37 (m, 4H), 2.45-2.29 (m, 1H), 2.14-1.70 (m, 6H), 1.66-1.50 (m, 1H), 1.39-1.18 (m, 11H), 1.15-1.08 (m, 4H), 0.93-0.78 (m, 1H).

Example 176 5-(6-(((R*)-1-Cyclobutylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(1-cyclobutylethyl)-4-(trifluoromethyl)pyridine-2-amine (Intermediate 89) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. A purification was performed via chiral SFC (Stationary phase: Chiralpak IC, 5 μm, 250×20 mm, Mobile phase: 0.5% iPrNH₂, 85% CO₂, 15% MeOH/iPrOH (50/50), first eluting peak) to separate enantiomers. MS (ESI): mass calcd. for C₂₆H₃₄F₃N₅O₃S, 553.2; m/z found, 554.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.16 (s, 1H), 7.64-7.49 (m, 1H), 6.61 (s, 1H), 4.74 (d, J=7.9 Hz, 1H), 4.34-4.15 (m, 1H), 3.92-3.76 (m, 1H), 3.65-3.36 (m, 4H), 2.42-2.34 (m, 1H), 2.13-1.45 (m, 7H), 1.43-1.19 (m, 11H), 1.18-1.06 (m, 4H), 0.90-0.82 (m, 1H).

Example 177 (S)-5-(6-((Dicyclopropylmethyl)amino)-4-(difluoromethyl)pyridine-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(dicyclopropylmethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 92) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₇H₃₃F₄N₅O₃S, 583.2; m/z found, 584.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 7.96 (d, J=9.9 Hz, 1H), 7.55-7.45 (m, 1H), 6.95-6.32 (m, 2H), 4.90 (d, J=7.9 Hz, 1H), 4.73-4.44 (m, 1H), 4.15-3.98 (m, 1H), 3.97-3.76 (m, 1H), 3.59-3.38 (m, 2H), 3.28-3.15 (m, 1H), 2.65-2.49 (m, 1H), 2.24-1.79 (m, 2H), 1.43-1.17 (m, 9H), 1.05-0.95 (m, 2H), 0.63-0.21 (m, 8H).

Example 178 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-((dicyclopropylmethyl)amino)-4-(difluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 70) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(dicyclopropylmethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 92) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₈H₃₅F₂N₅O₃S, 559.2; m/z found, 560.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 7.99 (s, 1H), 7.61-7.58 (m, 1H), 6.88-6.63 (m, 2H), 4.88 (d, J=8.0 Hz, 1H), 4.71-4.68 (m, 1H), 4.25 (t, J=4.9 Hz, 1H), 3.48 (d, J=6.3 Hz, 2H), 3.24 (q, J=7.4 Hz, 1H), 2.03-2.00 (m, 1H), 1.81-1.72 (m, 2H), 1.67-1.52 (m, 2H), 1.50-1.39 (m, 4H), 1.32 (s, 6H), 1.07-0.95 (m, 2H), 0.59-0.29 (m, 8H).

Example 179 (S)-5-(6-((Dicyclopropylmethyl)amino)-4-(difluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(dicyclopropylmethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 92) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₇H₃₅F₂N₅O₃S, 547.2; m/z found, 548.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 7.99-7.95 (m, 1H), 7.59-7.53 (m, 1H), 7.00-6.59 (m, 2H), 4.90-4.87 (m, 1H), 4.30-4.20 (m, 1H), 3.65-3.33 (m, 4H), 3.29-3.18 (m, 1H), 2.11-1.70 (m, 4H), 1.59-1.51 (m, 1H), 1.32 (d, J=1.6 Hz, 6H), 1.23 (d, J=6.3 Hz, 2H), 1.06-0.94 (m, 3H), 0.60-0.27 (m, 8H).

Example 180 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-(methyl-d₃)propyl-3,3,3-d₃)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)—N-(2-hydroxy-2-(methyl-d₃)propyl-3,3,3-d₃)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 77) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 41) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₂₆D₆F₃N₅O₃S, 533.2; m/z found, 534.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17 (s, 1H), 7.65-7.51 (m, 1H), 6.63 (s, 1H), 4.89 (s, 1H), 4.32-4.15 (m, 1H), 3.63-3.34 (m, 4H), 2.13-1.68 (m, 4H), 1.65-1.45 (m, 10H), 1.32-1.07 (m, 3H).

Example 181 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl-1,1-d₂)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (S)—N-(2-hydroxy-2-methylpropyl-1,1-d₂)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 76) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide and 5-bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 41) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₃₀D₂F₃N₅O₃S, 529.2; m/z found, 530.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.18 (s, 1H), 7.59-7.52 (m, 1H), 6.63 (s, 1H), 4.88 (s, 1H), 4.30-4.26 (m, 0.25H), 4.24-4.16 (m, 0.75H), 3.66-3.34 (m, 2H), 2.09-2.04 (m, 1H), 2.03-1.81 (m, 1H), 1.76-1.70 (m, 1H), 1.66-1.57 (m, 1H), 1.57-1.48 (m, 1H), 1.46 (s, 9H), 1.31 (s, 6H), 1.28-1.22 (m, 2.5H), 1.11 (d, J=6.4 Hz, 0.5H).

Example 182 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(cis-4-hydroxytetrahydrofuran-3-yl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridine-3-yl)thiazole-2-carboxamide

To a screw capped vial was added ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (150 mg, 0.28 mmol, Intermediate 93), cis-4-aminotetrahydrofuran-3-ol hydrochloride (197 mg, 1.4 mmol), ethanol (3.0 mL) and DIPEA (0.24 mL, 1.4 mmol). The vial was capped and the reaction heated to 80° C. for 24 h. The solvent was removed under reduced pressure, crude residue re-dissolved in DCM and purified by FCC (0-100% ethyl acetate/DCM) to provide the title compound. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₄S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.13 (s, 1H), 7.76-7.66 (m, 1H), 6.51 (s, 1H), 4.73-4.42 (m, 3H), 4.23-3.68 (m, 6H), 2.68-2.46 (m, 2H), 2.33-2.21 (m, 2H), 2.20-1.87 (m, 6H), 1.55 (s, 3H), 1.41-1.22 (m, 3H).

Example 183 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-((3R*,4R*)-4-hydroxytetrahydrofuran-3-yl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridine-3-yl)thiazole-2-carboxamide

The title compound was isolated by purification of Example 182 by chiral SFC (Stationary phase: CHIRALPAK IC, 5 μm, 250×20 mm, Mobile phase: 85% CO₂, 15% methanol, 0.3% iPrNH₂). MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₄S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (600 MHz, CDCl₃) δ 8.14 (s, 1H), 7.76-7.71 (m, 1H), 6.51 (s, 1H), 5.23 (s, 1H), 4.69-4.56 (m, 1.2H), 4.55-4.45 (m, 1.8H), 4.20 (dd, J=8.9, 7.5 Hz, 1H), 4.15-4.01 (m, 2H), 3.94-3.86 (m, 1.8H), 3.85-3.70 (m, 1.2H), 2.60-2.50 (m, 1H), 2.31-2.25 (m, 2H), 2.19-2.02 (m, 3H), 2.01-1.89 (m, 2H), 1.55 (s, 3H), 1.36-1.30 (m, 3H), 1.22 (d, J=6.2 Hz, 0.3H), 1.09 (d, J=6.2 Hz, 0.7H).

Example 184 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-((3S*,4S*)-4-hydroxytetrahydrofuran-3-yl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridine-3-yl)thiazole-2-carboxamide

The title compound was isolated by purification of Example 182 by chiral SFC (Stationary phase: CHIRALPAK IC, 5 μm, 250×20 mm, Mobile phase: 85% CO₂, 15% methanol, 0.3% iPrNH₂). MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₄S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (600 MHz, CDCl₃) δ 8.14 (s, 1H), 7.76-7.71 (m, 1H), 6.51 (s, 1H), 5.23 (s, 1H), 4.69-4.56 (m, 1.2H), 4.55-4.45 (m, 1.8H), 4.20 (dd, J=8.9, 7.5 Hz, 1H), 4.15-4.01 (m, 2H), 3.94-3.86 (m, 1.8H), 3.85-3.70 (m, 1.2H), 2.60-2.50 (m, 1H), 2.31-2.25 (m, 2H), 2.19-2.02 (m, 3H), 2.01-1.89 (m, 2H), 1.55 (s, 3H), 1.36-1.30 (m, 3H), 1.22 (d, J=6.2 Hz, 0.3H), 1.09 (d, J=6.2 Hz, 0.7H).

Example 185 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-((3S,4R)-4-hydroxytetrahydrofuran-3-yl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridine-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (3S,4R)-4-aminotetrahydrofuran-3-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₄S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.14 (s, 1H), 7.26-7.19 (m, 1H), 6.51 (s, 1H), 5.29 (s, 1H), 4.63-4.34 (m, 3H), 4.28-3.70 (m, 6H), 3.20-3.10 (m, 1H), 2.64-2.46 (m, 1H), 2.34-2.21 (m, 2H), 2.20-1.87 (m, 5H), 1.55 (s, 3H), 1.38 (d, J=6.4 Hz, 2H), 1.29-1.18 (m, 1H).

Example 186 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-((3R,4S)-4-hydroxytetrahydrofuran-3-yl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridine-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (3R,4S)-4-aminotetrahydrofuran-3-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₄S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.14 (s, 1H), 7.26-7.19 (m, 1H), 6.51 (s, 1H), 5.29 (s, 1H), 4.63-4.34 (m, 3H), 4.28-3.70 (m, 6H), 3.20-3.10 (m, 1H), 2.64-2.46 (m, 1H), 2.34-2.21 (m, 2H), 2.20-1.87 (m, 5H), 1.55 (s, 3H), 1.38 (d, J=6.4 Hz, 2H), 1.29-1.18 (m, 1H).

Example 187 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using 4-aminotetrahydro-2H-thiopyran-1,1-dioxide in place of (S)-3-amino-2-methylbutan-2-ol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₄S₂, 609.2; m/z found, 610.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.04 (m, 1H), 7.22-6.61 (m, 3H), 5.02-4.82 (m, 2H), 4.30-4.17 (m, 2H), 3.64-3.52 (m, 0.7H), 3.49-3.28 (m, 1.3H), 3.27-3.07 (m, 4H), 2.51-2.23 (m, 4H), 2.13-1.72 (m, 3H), 1.60-1.52 (m, 1H), 1.42 (d, J=6.7 Hz, 3H), 1.25 (d, J=6.8 Hz, 2H), 1.01 (d, J=6.4 Hz, 1H).

Example 188 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-N-((1r,3S)-3-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (1r,3R)-3-aminocyclobutan-1-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.2; m/z found, 548.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.03 (m, 1H), 7.35-7.22 (m, 1H), 7.05-6.60 (m, 2H), 5.01-4.84 (m, 2H), 4.72-4.54 (m, 2H), 4.30-4.08 (m, 1H), 3.63-3.52 (m, 0.7H), 3.49-3.29 (m, 1.3H), 2.52-2.40 (m, 4H), 2.13-1.48 (m, 4H), 1.42 (d, J=6.4 Hz, 3H), 1.30-1.18 (m, 3H), 1.01 (d, J=6.4 Hz, 1H).

Example 189 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)-N—((S-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

To a screw capped vial was added ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate (100 mg, 0.20 mmol, Intermediate 95), (S)-3-amino-2-methylbutan-2-ol (105 mg, 1.0 mmol) and ethanol (2.0 mL). The vial was capped and the reaction heated to 80° C. for 24 h. The solvent was removed under reduced pressure, crude residue re-dissolved in DCM and purified by FCC (0-100% ethyl acetate/DCM) to provide the title compound. MS (ESI): mass calcd. for C₂₇H₃₅F₂N₅O₃S, 547.2; m/z found, 547.8 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.04 (s, 1H), 7.43 (d, J=9.3 Hz, 1H), 6.52 (s, 2H), 5.14 (s, 1H), 4.69 (t, J=4.8 Hz, 1H), 4.22 (t, J=4.5 Hz, 1H), 4.16-4.03 (m, 1H), 2.30-2.22 (m, 2H), 2.17-2.10 (m, 2H), 1.99-1.87 (m, 3H), 1.85-1.69 (m, 2H), 1.55-1.53 (m, 4H), 1.49-1.38 (m, 5H), 1.34-1.22 (m, 9H).

Example 190 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((3S,4R)-4-hydroxytetrahydrofuran-3-yl)-thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (3R,3S)-4-aminotetrahydrofuran-3-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxylate (Intermediate 96) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₄F₇N₅O₄S, 599.1; m/z found, 600.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.08-8.03 (m, 1H), 7.31-7.16 (m, 1H), 6.96-6.52 (m, 2H), 5.03-4.83 (m, 2H), 4.71-4.64 (m, 0.25H), 4.53-4.44 (m, 1.75H), 4.42-4.36 (m, 1H), 4.26-4.14 (m, 2H), 4.13-3.97 (m, 1H), 3.96-3.72 (m, 3H), 3.00 (s, 1H), 2.72-2.47 (m, 1H), 2.20-2.00 (m, 1H), 1.43-1.35 (m, 5.5H), 1.17 (d, J=6.5 Hz, 0.5H).

Example 191 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-N-((1r,3S)-3-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (1r,3R)-3-aminocyclobutan-1-ol in place in place of (S)-3-amino-2-methylbutan-2-ol and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1,-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxylate (Intermediate 96) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₄F₇N₅O₃S, 583.1; m/z found, 584.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.08-8.04 (m, 1H), 7.21-7.16 (m, 1H), 6.92-6.55 (m, 2H), 5.00-4.90 (m, 1H), 4.82 (d, J=9.5 Hz, 1H), 4.73-4.57 (m, 2.3H), 4.54-4.46 (m, 0.7H), 4.08-3.98 (m, 1H), 3.92-3.78 (m, 1H), 2.65-2.40 (m, 5H), 2.23-2.02 (m, 1H), 1.84 (d, J=4.4 Hz, 1H), 1.42 (d, J=6.9 Hz, 3H), 1.36 (d, J=6.5 Hz, 2.3H), 1.31-1.15 (m, 0.7H).

Example 192 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-N-(1,1-dioxidothietan-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 182, using 3-aminothietan-1,1-dioxide in place in place of (rac)-4-aminotetrahydrofuran-3-ol and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1,-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxylate (Intermediate 96) in place of ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₂H₂₂F₇N₅O₄S₂, 617.1; m/z found, 618.0 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.08-8.04 (m, 1H), 7.68-7.64 (m, 1H), 6.92-6.56 (m, 2H), 5.03-4.87 (m, 2H), 4.78 (d, J=9.6 Hz, 1H), 4.73-4.59 (m, 2.3H), 4.55-4.45 (m, 0.7H), 4.23-3.98 (m, 1H), 3.91-3.77 (m, 1H), 3.65 (s, 2H), 2.74-2.49 (m, 1H), 2.25-2.00 (m, 1H), 1.43-1.36 (m, 3H), 1.24 (d, J=17.1 Hz, 2.5H), 0.87 (dd, J=16.5, 9.8 Hz, 0.5H).

Example 193 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(difluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using ethyl 5-(6-(((S)-1-cyclopropylethyl)amino)-4-(difluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 97) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₃F₄N₅O₃S, 571.2; m/z found, 572.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 7.99-7.97 (m, 1H), 7.40-7.33 (m, 1H), 6.93-6.53 (m, 2H), 4.94 (d, J=7.5 Hz, 1H), 4.72-4.66 (m, 0.3H), 4.58-4.45 (m, 0.7H), 4.17-3.98 (m, 2H), 3.96-3.77 (m, 1H), 3.41-3.35 (m, 1H), 2.69-2.45 (m, 1H), 2.23-1.99 (m, 1H), 1.87-1.81 (m, 1H), 1.44-1.18 (m, 15H), 1.03-0.80 (m, 1H), 0.61-0.45 (m, 2H), 0.41-0.22 (m, 2H).

Example 194 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(difluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (R)-3-amino-2-methylbutan-2-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl 5-(6-(((S)-1-cyclopropylethyl)amino)-4-(difluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 97) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₃F₄N₅O₃S, 571.2; m/z found, 572.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 7.99-7.97 (m, 1H), 7.40-7.33 (m, 1H), 6.93-6.53 (m, 2H), 4.94 (d, J=7.5 Hz, 1H), 4.72-4.66 (m, 0.3H), 4.58-4.45 (m, 0.7H), 4.17-3.98 (m, 2H), 3.96-3.77 (m, 1H), 3.41-3.35 (m, 1H), 2.69-2.45 (m, 1H), 2.23-1.99 (m, 1H), 1.87-1.81 (m, 1H), 1.44-1.18 (m, 15H), 1.03-0.80 (m, 1H), 0.61-0.45 (m, 2H), 0.41-0.22 (m, 2H).

Example 195 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridine-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate in place of ethyl 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.16-8.13 (m, 1H), 7.34 (d, J=9.2 Hz, 1H), 6.51 (s, 1H), 5.21 (s, 1H), 4.62-4.47 (m, 1H), 4.17-3.77 (m, 3H), 2.62-2.46 (m, 1H), 2.33-2.22 (m, 2H), 2.20-1.77 (m, 6H), 1.56 (s, 3H), 1.38-1.22 (m, 12H).

Example 196 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridine-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (R)-3-amino-2-methylbutan-2-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(6-((1-methylcyclobutyl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate in place of ethyl 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.14 (s, 1H), 7.36 (d, J=9.3 Hz, 1H), 6.51 (s, 1H), 5.21 (s, 1H), 4.70-4.64 (m, 0.3H), 4.55-4.44 (m, 0.7H), 4.18-3.96 (m, 2H), 3.95-3.74 (m, 1H), 2.64-2.46 (m, 1H), 2.34-2.22 (m, 2H), 2.21-2.01 (m, 3H), 2.00-1.76 (m, 3H), 1.56 (d, J=13.5 Hz, 3H), 1.41-1.19 (m, 12H).

Example 197 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxylate (Intermediate 96) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₇N₅O₃S, 599.2; m/z found, 600.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.07-8.03 (m, 1H), 7.37-7.34 (m, 1H), 6.92-6.54 (m, 2H), 5.03-4.71 (m, 2.3H), 4.56-4.44 (m, 0.7H), 4.17-4.01 (m, 2.3H), 3.96-3.77 (m, 0.7H), 2.71-2.46 (m, 1H), 2.24-1.97 (m, 1H), 1.85-1.75 (m, 1H), 1.46-1.18 (m, 15H).

Example 198 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (R)-3-amino-2-methylbutan-2-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxylate (Intermediate 96) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₇N₅O₃S, 599.2; m/z found, 600.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.07-8.03 (m, 1H), 7.37-7.34 (m, 1H), 6.92-6.54 (m, 2H), 5.03-4.71 (m, 2.3H), 4.56-4.44 (m, 0.7H), 4.17-4.01 (m, 2.3H), 3.96-3.77 (m, 0.7H), 2.71-2.46 (m, 1H), 2.24-1.97 (m, 1H), 1.85-1.75 (m, 1H), 1.46-1.18 (m, 15H).

Example 199 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-N—((S)-3-hydroxy-3-methylburan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S, 563.2; m/z found, 564.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.04 (m, 1H), 7.41-7.36 (m, 1H), 7.03-6.62 (m, 2H), 5.01-4.82 (m, 2H), 4.39-4.33 (m, 0.3H), 4.26-4.03 (m, 1.7H), 3.65-3.46 (m, 1.4H), 3.43-3.35 (m, 0.6H), 2.13-1.49 (m, 5H), 1.41 (d, J=6.7 Hz, 3H), 1.36-1.18 (m, 11H), 1.07 (d, J=6.4 Hz, 1H).

Example 200 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-N—((R)-3-hydroxy-3-methylburan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (R)-3-amino-2-methylbutan-2-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S, 563.2; m/z found, 564.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.04 (m, 1H), 7.41-7.36 (m, 1H), 7.03-6.62 (m, 2H), 5.01-4.82 (m, 2H), 4.39-4.33 (m, 0.3H), 4.26-4.03 (m, 1.7H), 3.65-3.46 (m, 1.4H), 3.43-3.35 (m, 0.6H), 2.13-1.49 (m, 5H), 1.41 (d, J=6.7 Hz, 3H), 1.36-1.18 (m, 11H), 1.07 (d, J=6.4 Hz, 1H).

Example 201 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-((1R,2S)-2-hydroxycyclopentyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (1S,2R)-2-aminocyclopentan-1-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl 5-(6-(((S)-1-cyclopropylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 98) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₀F₅N₅O₃S, 587.2; m/z found, 588.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12 (s, 1H), 7.56 (dd, J=16.1, 8.1 Hz, 1H), 6.61 (s, 1H), 4.99 (d, J=7.4 Hz, 1H), 5.02-4.97 (m, 0.3H), 4.52-4.43 (m, 0.7H), 4.37-4.20 (m, 2H), 4.18-3.99 (m, 1H), 3.44-3.33 (m, 1H), 2.60-2.47 (m, 1H), 2.25-1.87 (m, 4H), 1.83-1.60 (m, 4H), 1.41-1.21 (m, 7H), 1.00-0.85 (m, 1H), 0.62-0.46 (m, 2H), 0.41-0.23 (m, 2H).

Example 202 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using ethyl 5-(6-(((S)-1-cyclopropylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 98) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.2; m/z found, 590.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12 (s, 1H), 7.35 (d, J=9.3 Hz, 1H), 6.61 (s, 1H), 5.02 (d, J=7.5 Hz, 1H), 4.65-4.45 (m, 1H), 4.18-3.71 (m, 3H), 3.43-3.38 (m, 1H), 2.65-2.44 (m, 1H), 2.21-1.99 (m, 1H), 1.88-1.80 (m, 1H), 1.44-1.21 (m, 15H), 1.00-0.90 (m, 1H), 0.62-0.45 (m, 2H), 0.42-0.23 (m, 2H).

Example 203 5-(6-(((S)-1-Cyclopropylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 189, using (R)-3-amino-2-methylbutan-2-ol in place of (S)-3-amino-2-methylbutan-2-ol and ethyl 5-(6-(((S)-1-cyclopropylethyl)amino)-4-(trifluoromethyl)pyridine-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 98) in place of ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridine-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.2; m/z found, 590.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12 (s, 1H), 7.37 (d, J=9.2 Hz, 1H), 6.61 (s, 1H), 5.02 (d, J=7.5 Hz, 1H), 4.75-4.65 (m, 0.3H), 4.53-4.44 (m, 0.7H), 4.19-3.73 (m, 3H), 3.45-3.35 (m, 1H), 2.66-2.44 (m, 1H), 2.25-1.80 (m, 2H), 1.47-1.18 (m, 14H), 1.06-0.75 (m, 2H), 0.63-0.45 (m, 2H), 0.43-0.22 (m, 2H).

Example 204 5-(4-(Difluoromethyl)-6-(((1R)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((3R,4S)-4-hydroxytetrahydrofuran-3-yl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 5-(4-(difluoromethyl)-6-(((R)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 104: Step B) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (3S,4R)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₄S, 577.6; m/z found, 578.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.01 (m, 1H), 7.37-7.27 (m, 1H), 7.02-6.64 (m, 2H), 4.92-4.71 (m, 2H), 4.49-4.36 (m, 2H), 4.24-4.13 (m, 3H), 3.89-3.73 (m, 2H), 3.62-3.32 (m, 3H), 2.04-1.90 (m, 3H), 1.83-1.50 (m, 3H), 1.23-1.18 (d, J=6.3 Hz, 2H), 1.08-1.00 (m, 4H).

Example 205 5-(4-(Difluoromethyl)-6-(((1R)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1r,3S)-3-hydroxycyclobutyl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting ethyl 5-(4-(difluoromethyl)-6-(((R)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 104: Step B) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and trans-3-aminocyclobutanol HCl for 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 562.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 7.36-7.27 (m, 1H), 7.03-6.64 (m, 2H), 4.92-4.72 (m, 2H), 4.71-4.55 (m, 2H), 4.28-4.17 (m, 1H), 3.62-3.31 (m, 2H), 2.51-2.38 (m, 4H), 2.22-2.16 (d, J=4.2 Hz, 1H), 2.04-1.84 (m, 3H), 1.81-1.71 (m, 1H), 1.67-1.49 (m, 2H), 1.22-1.19 (d, J=6.3 Hz, 2H), 1.07-1.00 (m, 4H).

Example 206 5-(4-(Difluoromethyl)-6-(((1R)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1R)-2-hydroxy-1-methyl-ethyl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 5-(4-(difluoromethyl)-6-(((R)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 104: Step B) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₈F₅N₅O₃S, 549.6; m/z found, 550.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 7.35-7.27 (m, 1H), 7.03-6.64 (m, 2H), 4.91-4.72 (m, 2H), 4.31-4.16 (m, 2H), 3.83-3.64 (m, 2H), 3.61-3.33 (m, 2H), 2.57-2.50 (m, 1H), 2.03-1.85 (m, 3H), 1.81-1.72 (m, 1H), 1.67-1.49 (m, 2H), 1.35-1.31 (d, J=6.8 Hz, 3H), 1.22-1.19 (d, J=6.3 Hz, 2H), 1.08-1.01 (m, 4H).

Example 207 5-(4-(Difluoromethyl)-6-(((1R)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((3S,4R)-4-hydroxytetrahydrofuran-3-yl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 5-(4-(difluoromethyl)-6-(((R)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 104: Step B) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (3R,4S)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₄S, 577.6; m/z found, 578.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09-8.00 (m, 1H), 7.36-7.27 (m, 1H), 7.05-6.65 (m, 2H), 4.91-4.70 (m, 2H), 4.47-4.36 (m, 2H), 4.28-4.13 (m, 3H), 3.90-3.73 (m, 2H), 3.63-3.30 (m, 3H), 2.04-1.90 (m, 3H), 1.81-1.52 (m, 3H), 1.24-1.21 (d, J=6.3 Hz, 2H), 1.08-1.02 (m, 3H), 1.01-0.97 (d, J=6.4 Hz, 1H).

Example 208 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((3R,4S)-4-hydroxytetrahydrofuran-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (3S,4R)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₄S, 589.6; m/z found, 590.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.11-8.06 (s, 1H), 7.40-7.35 (d, J=6.8 Hz, 1H), 6.89-6.65 (m, 2H), 4.95-4.64 (m, 3H), 4.46-4.36 (m, 2H), 4.24-4.19 (m, 1H), 4.15-4.10 (m, 2H), 1.56-1.49 (m, 1H), 3.87-3.74 (m, 2H), 3.49-3.44 (d, J=3.1 Hz, 1H), 2.02-1.93 (m, 1H), 1.80-1.68 (m, 2H), 1.66-1.57 (m, 1H), 1.48-1.40 (m, 5H), 1.06-1.02 (m, 3H).

Example 209 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((3S,4R)-4-hydroxytetrahydrofuran-3-yl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (3R,4S)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₄S, 589.6; m/z found, 590.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.06 (s, 1H), 7.41-7.36 (d, J=6.8 Hz, 1H), 6.89-6.65 (m, 2H), 4.95-4.64 (m, 3H), 4.48-4.36 (m, 2H), 4.24-4.19 (m, 1H), 4.15-4.10 (m, 2H), 3.87-3.74 (m, 2H), 3.51-3.46 (m, 1H), 2.02-1.94 (m, 1H), 1.80-1.68 (m, 2H), 1.66-1.57 (m, 1H), 1.52-1.38 (m, 6H), 1.07-1.01 (m, 3H).

Example 210 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1S,2S)-2-hydroxycyclopentyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting ethyl 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (1S,2S)-trans-2-aminocyclopentanol HCl for 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₆H₃₀F₅N₅O₃S, 587.6; m/z found, 588.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.07 (s, 1H), 7.34-7.29 (d, J=5.3 Hz, 1H), 6.90-6.65 (m, 2H), 4.94-4.65 (m, 3H), 4.19-4.12 (m, 2H), 4.08-4.02 (m, 1H), 3.90-3.87 (m, 1H), 2.32-2.23 (m, 1H), 2.13-2.06 (m, 1H), 2.01-1.93 (m, 1H), 1.91-1.83 (m, 1H), 1.81-1.77 (m, 1H), 1.75-1.70 (m, 2H), 1.65-1.58 (m, 2H), 1.49-1.38 (m, 6H), 1.07-1.01 (m, 3H).

Example 211 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1R*,2S*)-2-hydroxycyclopropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 157 substituting N-((1R*,2S*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 101: Step F1) for N-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 548.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-7.99 (m, 1H), 7.52-7.44 (m, 1H), 7.01-6.65 (m, 2H), 4.82-4.71 (m, 2H), 4.37-4.16 (m, 1H), 3.77-3.34 (m, 3H), 2.99-2.83 (m, 2H), 2.03-1.83 (m, 3H), 1.81-1.72 (m, 1H), 1.66-1.62 (m, 1H), 1.57-1.49 (m, 1H), 1.23-1.20 (d, J=6.3 Hz, 2H), 1.16-1.11 (m, 1H), 1.07-1.02 (m, 3H), 1.02-1.00 (d, J=6.4 Hz, 1H), 0.80-0.75 (m, 1H).

Example 212 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1S*,2R*)-2-hydroxycyclopropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 157 substituting N-((1S*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 101: Step F2) for N-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 548.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.52-7.43 (m, 1H), 7.01-6.65 (m, 2H), 4.82-4.72 (m, 2H), 4.37-4.17 (m, 1H), 3.77-3.35 (m, 3H), 2.94-2.82 (m, 2H), 2.03-1.73 (m, 4H), 1.67-1.61 (m, 1H), 1.56-1.50 (m, 1H), 1.22-1.19 (d, J=6.3 Hz, 2H), 1.17-1.12 (m, 1H), 1.07-1.01 (m, 4H), 0.82-0.76 (m, 1H).

Example 213 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1R*,2R*)-2-hydroxycyclopropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 157 substituting N-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 101: Step G1) for N-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 548.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.08-8.00 (m, 1H), 7.18-7.08 (m, 1H), 7.01-6.66 (m, 2H), 4.81-4.72 (m, 2H), 4.31-4.16 (m, 1H), 3.64-3.19 (m, 4H), 2.94-2.86 (m, 1H), 2.09-2.04 (m, 1H), 2.03-1.86 (m, 3H), 1.80-1.71 (m, 1H), 1.66-1.50 (m, 2H), 1.22-1.19 (d, J=6.3 Hz, 2H), 1.07-1.02 (m, 3H), 1.01-0.95 (m, 2H).

Example 214 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclopropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 157 substituting N-((1S*,2S*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 101: Step G2) for N-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 548.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 7.20-7.10 (m, 1H), 7.00-6.65 (m, 2H), 4.85-4.73 (m, 2H), 4.27-4.16 (m, 1H), 3.65-3.23 (m, 4H), 2.94-2.87 (m, 1H), 2.03-1.85 (m, 4H), 1.79-1.59 (m, 2H), 1.56-1.50 (m, 1H), 1.22-1.19 (d, J=6.3 Hz, 2H), 1.07-1.02 (m, 3H), 1.01-0.96 (m, 2H).

Example 215 5-(4-(Difluoromethyl)-6-(((1S)-2,2,2-trifluoro-1-methyl-ethyl)amino)-3-pyridyl)-N-((3R,4S)-4-hydroxytetrahydrofuran-3-yl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3S,4R)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₄S, 563.5; m/z found, 564.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.11-8.02 (m, 1H), 7.36-7.27 (m, 1H), 6.98-6.63 (m, 2H), 4.99-4.89 (m, 2H), 4.48-4.41 (m, 1H), 4.40-4.35 (m, 1H), 4.25-4.14 (m, 3H), 3.89-3.83 (m, 1H), 3.78-3.73 (m, 1H), 3.60-3.26 (m, 3H), 2.10-2.05 (m, 1H), 1.96-1.87 (m, 1H), 1.80-1.78 (m, 1H), 1.68-1.52 (m, 1H), 1.44-1.39 (d, J=6.3 Hz, 3H), 1.24-1.21 (d, J=6.3 Hz, 2H), 1.03-1.00 (d, J=6.4 Hz, 1H).

Example 216 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((2R*,3R*)-3-hydroxybutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-aminobutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralcel OD-H, 5 μm, 250×30 mm, Mobile phase: 14% iPrOH+0.3% iPrNH₂, 86% CO₂, first eluting diastereomer) followed by a second SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 10% iPrOH+0.3% iPrNH₂, 90% CO₂, second eluting diastereomer). MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S, 563.6; m/z found, 564.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.40-7.32 (m, 1H), 7.07-6.66 (m, 2H), 4.85-4.67 (m, 2H), 4.32-3.98 (m, 3H), 3.60-3.34 (m, 2H), 2.08-1.97 (m, 2H), 1.93-1.86 (m, 1H), 1.80-1.72 (m, 1H), 1.65-1.60 (m, 1H), 1.56-1.50 (m, 1H), 1.28-1.20 (m, 9H), 1.08-1.02 (m, 4H).

Example 217 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((2S*,3S*)-3-hydroxybutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-aminobutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralcel OD-H, 5 μm, 250×30 mm, Mobile phase: 14% i-PrOH+0.3% i-PrNH₂, 86% CO₂, first eluting diastereomer) followed by a second SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 10% iPrOH+0.3% iPrNH₂, 90% CO₂, first eluting diastereomer). MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S, 563.6; m/z found, 564.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.01 (m, 1H), 7.38-7.31 (m, 1H), 7.06-6.66 (m, 2H), 4.83-4.68 (m, 2H), 4.35-3.87 (m, 3H), 3.60-3.35 (m, 2H), 2.08-2.01 (m, 1H), 1.98-1.89 (m, 2H), 1.80-1.74 (m, 1H), 1.65-1.53 (m, 2H), 1.36-1.31 (d, J=6.8 Hz, 3H), 1.29-1.25 (d, J=6.3 Hz, 3H), 1.23-1.20 (m, 3H), 1.08-1.02 (m, 4H).

Example 218 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((2R*,3S*)-3-hydroxybutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-aminobutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralcel OD-H, 5 μm, 250×30 mm, Mobile phase: 14% iPrOH+0.3% iPrNH₂, 86% CO₂, second eluting diastereomer) followed by a second SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×20 mm, Mobile phase: 15% i-PrOH+0.3% iPrNH₂, 85% CO₂). MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S, 563.6; m/z found, 564.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 7.39-7.30 (m, 1H), 7.03-6.68 (m, 2H), 4.83-4.65 (m, 2H), 4.30-3.99 (m, 3H), 3.61-3.33 (m, 2H), 2.07-1.75 (m, 4H), 1.65-1.61 (m, 1H), 1.54-1.50 (m, 1H), 1.29-1.24 (m, 6H), 1.22-1.20 (m, 3H), 1.08-1.02 (m, 4H).

Example 219 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((2S*,3R*)-3-hydroxybutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-aminobutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralcel OD-H, 5 μm, 250×30 mm, Mobile phase: 14% iPrOH+0.3% iPrNH₂, 86% CO₂, third eluting diastereomer). MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S, 563.6; m/z found, 564.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.01 (m, 1H), 7.37-7.29 (m, 1H), 7.07-6.66 (m, 2H), 4.84-4.65 (m, 2H), 4.33-3.86 (m, 3H), 3.62-3.33 (m, 2H), 2.08-1.75 (m, 5H), 1.67-1.62 (m, 1H), 1.36-1.32 (m, 3H), 1.30-1.25 (m, 4H), 1.24-1.21 (d, J=6.3 Hz, 2H), 1.08-1.02 (m, 4H).

Example 220 5-(4-(Difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((3R,4S)-4-hydroxytetrahydrofuran-3-yl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3S,4R)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₄S, 577.6; m/z found, 578.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.02 (m, 1H), 7.39-7.28 (m, 1H), 7.04-6.63 (m, 2H), 4.96-4.89 (d, J=9.8 Hz, 1H), 4.84-4.71 (m, 1H), 4.48-4.35 (m, 2H), 4.25-4.14 (m, 3H), 3.91-3.74 (m, 2H), 3.60-3.30 (m, 3H), 2.10-1.92 (m, 3H), 1.83-1.71 (m, 1H), 1.67-1.50 (m, 2H), 1.23-1.20 (d, J=6.3 Hz, 2H), 1.07-1.02 (m, 3H), 1.02-0.98 (d, J=6.4 Hz, 1H).

Example 221 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-2,2,2-trifluoro-1-methyl-ethyl)amino)-3-pyridyl)-N-((1r,3S)-3-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-3-aminocyclobutanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1R,4R)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 117) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₆F₅N₅O₃S, 559.6; m/z found, 560.1 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.10-8.07 (s, 1H), 7.37-7.31 (d, J=7.1 Hz, 1H), 6.91-6.60 (m, 2H), 5.01-4.90 (m, 2H), 4.70-4.56 (m, 3H), 4.21-4.16 (m, 1H), 2.51-2.39 (m, 4H), 2.21-2.16 (d, J=4.5 Hz, 1H), 1.79-1.69 (m, 3H), 1.51-1.39 (m, 8H).

Example 222 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1r,3S)-3-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-3-aminocyclobutanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.6; m/z found, 574.1 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.11-8.05 (s, 1H), 7.41-7.35 (d, J=7.2 Hz, 1H), 6.92-6.62 (m, 2H), 4.94-4.88 (m, 1H), 4.84-4.55 (m, 4H), 4.15-4.08 (m, 1H), 2.51-2.39 (m, 4H), 2.25-2.18 (m, 1H), 2.02-1.93 (m, 1H), 1.81-1.69 (m, 4H), 1.66-1.56 (m, 1H), 1.46-1.41 (m, 4H), 1.07-1.01 (m, 3H).

Example 223 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclopropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 157 substituting trans-N-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 105) for N-((1R*,2R*)-2-((tert-butyldimethylsilyl)oxy)cyclopropyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₂H₂₄F₅N₅O₃S, 533.5; m/z found, 534.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.02 (m, 1H), 7.19-7.09 (m, 1H), 6.98-6.63 (m, 2H), 4.99-4.87 (m, 2H), 4.31-4.16 (m, 1H), 3.64-3.28 (m, 4H), 2.94-2.86 (m, 1H), 2.08-2.04 (m, 1H), 1.96-1.87 (m, 1H), 1.79-1.50 (m, 2H), 1.43-1.40 (d, J=6.5 Hz, 3H), 1.27-1.26 (m, 1H), 1.23-1.20 (dd, J=6.3, 2.5 Hz, 2H), 1.02-0.96 (m, 2H).

Example 224 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-2,2,2-trifluoro-1-methyl-ethyl)amino)-3-pyridyl)-N-((1R,2R)-2-hydroxycyclopentyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,2R)-trans-2-aminocyclopentanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1R,4R)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 117) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.6; m/z found, 574.1 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.12-8.04 (s, 1H), 7.29-7.27 (m, 1H), 6.89-6.62 (m, 2H), 4.99-4.90 (m, 2H), 4.71-4.64 (m, 1H), 4.23-4.14 (m, 2H), 4.08-4.02 (m, 1H), 3.81-3.78 (m, 1H), 2.31-2.05 (m, 2H), 1.92-1.71 (m, 5H), 1.70-1.69 (s, 1H), 1.65-1.59 (m, 1H), 1.49-1.39 (m, 7H).

Example 225 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1R,2R)-2-hydroxycyclopentyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,2R)-trans-2-aminocyclopentanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₀F₅N₅O₃S, 587.6; m/z found, 588.1 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.11-8.06 (s, 1H), 7.31-7.27 (d, J=5.2 Hz, 1H), 6.90-6.64 (m, 2H), 4.89-4.64 (m, 3H), 4.19-4.02 (m, 3H), 3.82-3.78 (m, 1H), 2.31-2.06 (m, 2H), 2.01-1.84 (m, 2H), 1.80-1.73 (m, 4H), 1.66-1.57 (m, 2H), 1.48-1.38 (m, 5H), 1.07-1.01 (m, 3H).

Example 226 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-2,2,2-trifluoro-1-methyl-ethyl)amino)-3-pyridyl)-N-((1R)-2-hydroxy-1-methyl-ethyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 117) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 548.1 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.11-8.05 (s, 1H), 7.38-7.32 (d, J=7.9 Hz, 1H), 6.88-6.62 (m, 2H), 5.01-4.90 (m, 2H), 4.70-4.64 (m, 1H), 4.31-4.21 (m, 2H), 1.63-1.53 (m, 2H), 3.83-3.65 (m, 2H), 2.56-2.46 (s, 1H), 1.81-1.72 (m, 2H), 1.48-1.43 (m, 4H), 1.43-1.39 (d, J=6.4 Hz, 3H), 1.35-1.30 (d, J=6.8 Hz, 3H).

Example 227 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1R)-2-hydroxy-1-methyl-ethyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 562.1 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.10-8.05 (s, 1H), 7.40-7.34 (d, J=7.9 Hz, 1H), 6.90-6.64 (m, 2H), 4.94-4.87 (d, J=9.8 Hz, 1H), 4.84-4.62 (m, 2H), 4.28-4.16 (m, 2H), 3.83-3.65 (m, 2H), 2.60-2.52 (s, 1H), 2.02-1.91 (m, 1H), 1.75-1.69 (m, 2H), 1.66-1.49 (m, 3H), 1.47-1.39 (m, 4H), 1.34-1.30 (d, J=6.8 Hz, 3H), 1.07-1.00 (m, 3H).

Example 228 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-((3R*,4R*)-4-hydroxytetrahydrofuran-3-yl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

To a microwave vial under N₂ was added ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (178 mg, 0.33 mmol, Intermediate 116), cis-4-aminotetrahydro-3-furanol HCl (244 mg, 1.66 mmol), DIPEA (0.31 mL, 0.82 mmol) and EtOH (1.58 mL), and the reaction was stirred at 100° C. for 18 h. The reaction mixture was cooled to rt and partitioned between EtOAc (20 mL) and saturated aqueous NH₄Cl (20 mL). The layers were separated and the aqueous further extracted with EtOAc (2×15 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-100% EtOAc/Hexanes) to provide the title compound. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 25% iPrOH+0.3% iPrNH₂, 75% CO₂, second eluting enantiomer). MS (ESI): mass calcd. for C₂₄H₂₅F₆N₅O₄S, 593.5; m/z found, 594.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.21-8.16 (s, 1H), 7.86-7.79 (d, J=7.8 Hz, 1H), 6.74-6.68 (s, 1H), 5.25-5.17 (d, J=9.3 Hz, 1H), 5.02-4.91 (m, 1H), 4.69-4.46 (m, 4H), 4.22-4.16 (m, 1H), 1.49-1.45 (m, 3H), 4.10-4.04 (m, 1H), 3.90-3.85 (m, 1H), 3.76-3.70 (m, 1H), 1.86-1.61 (m, 5H), 1.42-1.38 (m, 3H), 1.22-1.20 (d, J=6.1 Hz, 1H).

Example 229 5-(4-(Difluoromethyl)-6-(((1S)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1S,2S)-2-hydroxycyclopentyl)-4-((2S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1S,2S)-trans-2-aminocyclopentanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.01 (m, 1H), 7.30-7.20 (m, 1H), 7.02-6.66 (m, 2H), 4.95-4.72 (m, 2H), 4.27-4.15 (m, 2H), 4.08-4.01 (m, 1H), 3.87-3.80 (s, 1H), 3.61-3.29 (m, 2H), 2.33-2.23 (m, 1H), 2.12-2.03 (m, 2H), 2.02-1.82 (m, 4H), 1.81-1.75 (m, 2H), 1.66-1.50 (m, 3H), 1.23-1.20 (d, J=6.3 Hz, 2H), 1.07-1.02 (m, 3H), 1.01-0.98 (d, J=6.4 Hz, 1H).

Example 230 5-(4-(Difluoromethyl)-6-(((1R)-1-(trifluoromethyl)propyl)amino)-3-pyridyl)-N-((1S)-2-hydroxy-1,2-dimethyl-propyl)-4-)(2S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting ethyl 5-(4-(difluoromethyl)-6-(((R)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 104: Step B) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (S)-3-amino-2-methylbutan-2-ol HCl for 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₅H₃₂F₅N₅O₃S, 577.6; m/z found, 578.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-8.00 (m, 1H), 7.43-7.35 (m, 1H), 7.01-6.67 (m, 2H), 4.91-4.83 (d, J=9.8 Hz, 1H), 4.82-4.72 (m, 1H), 4.28-4.08 (m, 2H), 3.63-3.37 (m, 2H), 2.02-1.85 (m, 3H), 1.83-1.73 (m, 1H), 1.66-1.50 (m, 2H), 1.32-1.28 (m, 9H), 1.27-1.23 (t, J=7.1 Hz, 1H), 1.23-1.18 (d, J=6.3 Hz, 2H), 1.10-1.07 (d, J=6.4 Hz, 1H), 1.07-1.02 (m, 3H).

Example 231 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R,2R)-2-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,2R)-trans-2-aminocyclopentanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.02 (m, 1H), 7.29-7.22 (m, 1H), 7.00-6.66 (m, 2H), 4.94-4.72 (m, 2H), 4.25-4.14 (m, 2H), 4.08-4.01 (m, 1H), 3.89-3.79 (s, 1H), 3.61-3.30 (m, 2H), 2.32-2.24 (m, 1H), 2.11-2.06 (m, 1H), 2.01-1.84 (m, 4H), 1.81-1.75 (m, 2H), 1.65-1.51 (m, 3H), 1.28-1.24 (t, J=7.1 Hz, 1H), 1.23-1.20 (d, J=6.3 Hz, 2H), 1.07-1.02 (m, 3H), 1.02-1.00 (d, J=6.4 Hz, 1H).

Example 232 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 4-aminotetrahydro-2H-thiopyran 1,1-dioxide for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₄S₂, 623.7; m/z found, 624.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.01 (m, 1H), 7.23-7.12 (m, 1H), 7.02-6.66 (m, 2H), 4.90-4.84 (m, 1H), 4.83-4.69 (m, 1H), 4.30-4.17 (m, 2H), 3.61-3.30 (m, 2H), 3.22-3.11 (m, 4H), 2.48-2.39 (m, 2H), 2.35-2.25 (m, 2H), 2.03-1.85 (m, 3H), 1.83-1.71 (m, 1H), 1.65-1.50 (m, 2H), 1.23-1.21 (d, J=6.3 Hz, 2H), 1.07-1.02 (m, 3H), 1.02-0.99 (d, J=6.4 Hz, 1H).

Example 233 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-((1r,3S)-3-hydroxycyclobutyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-3-aminocyclobutanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 562.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.36-7.27 (m, 1H), 7.01-6.66 (m, 2H), 4.91-4.85 (m, 1H), 4.84-4.70 (m, 1H), 4.70-4.56 (m, 2H), 4.26-4.17 (m, 1H), 3.60-3.31 (m, 2H), 2.50-2.39 (m, 4H), 2.17-2.09 (s, 1H), 2.04-1.84 (m, 3H), 1.80-1.71 (m, 1H), 1.64-1.50 (m, 2H), 1.23-1.19 (m, 2H), 1.07-0.99 (m, 4H).

Example 234 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R)-2-hydroxy-1-methyl-ethyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (5)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₈F₅N₅O₃S, 549.6; m/z found, 550.2 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.09-8.02 (m, 1H), 7.34-7.27 (m, 1H), 7.01-6.67 (m, 2H), 4.87-4.81 (m, 1H), 4.81-4.72 (m, 1H), 4.31-4.17 (m, 2H), 3.84-3.65 (m, 2H), 3.61-3.34 (m, 2H), 2.51-2.42 (m, 1H), 2.03-1.85 (m, 3H), 1.81-1.72 (m, 1H), 1.65-1.50 (m, 2H), 1.35-1.31 (d, J=6.8 Hz, 3H), 1.23-1.20 (dd, J=6.3, 4.3 Hz, 2H), 1.08-1.01 (m, 4H).

Example 235 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-((2R*,3S*)-3-hydroxybutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-aminobutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralcel OD-H, 5 μm, 250×30 mm, Mobile phase: 5% MeOH+0.3% iPrNH₂, 95% CO₂) followed by a second SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×20 mm, Mobile phase: 8% mixture of EtOH/iPrOH 50/50 v/v+0.3% iPrNH₂, 92% CO₂). MS (ESI): mass calcd. for C₂₄H₃₂F₃N₅O₃S, 527.6; m/z found, 528.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19-8.16 (m, 1H), 7.39-7.32 (m, 1H), 6.64-6.60 (m, 1H), 4.87-4.83 (s, 1H), 4.23-4.14 (m, 2H), 4.05-3.97 (m, 1H), 3.61-3.35 (m, 2H), 2.09-2.02 (m, 1H), 1.47-1.44 (m, 9H), 1.91-1.85 (m, 1H), 1.77-1.71 (m, 1H), 1.54-1.51 (m, 1H), 1.28-1.26 (m, 3H), 1.25-1.23 (m, 5H), 1.22-1.20 (m, 1H), 1.12-1.09 (d, J=6.4 Hz, 1H).

Example 236 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-((2S*,3S*)-3-hydroxybutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-aminobutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralcel OD-H, 5 μm, 250×30 mm, Mobile phase: 5% MeOH+0.3% iPrNH₂, 95% CO₂) followed by a second SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×20 mm, Mobile phase: 8% mixture of EtOH/iPrOH 50/50 v/v+0.3% iPrNH₂, 92% CO₂). MS (ESI): mass calcd. for C₂₄H₃₂F₃N₅O₃S, 527.6; m/z found, 528.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.22-8.13 (s, 1H), 7.38-7.30 (m, 1H), 6.68-6.58 (s, 1H), 4.93-4.81 (m, 1H), 4.30-4.06 (m, 2H), 3.92-3.84 (m, 1H), 3.61-3.36 (m, 2H), 2.09-2.03 (m, 1H), 1.46-1.45 (m, 9H), 1.92-1.84 (m, 1H), 1.80-1.69 (m, 1H), 1.54-1.50 (m, 1H), 1.34-1.32 (d, J=6.8 Hz, 3H), 1.28-1.26 (m, 2H), 1.25-1.20 (m, 4H), 1.13-1.10 (d, J=6.4 Hz, 1H).

Example 237 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-((2R*,3R*)-3-hydroxybutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-aminobutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralcel OD-H, 5 μm, 250×30 mm, Mobile phase: 5% MeOH+0.3% iPrNH₂, 95% CO₂). MS (ESI): mass calcd. for C₂₄H₃₂F₃N₅O₃S, 527.6; m/z found, 528.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19-8.16 (s, 1H), 7.38-7.30 (m, 1H), 6.63-6.61 (m, 1H), 4.87-4.83 (s, 1H), 4.24-4.05 (m, 2H), 3.92-3.86 (m, 1H), 3.60-3.37 (m, 2H), 2.09-2.02 (m, 1H), 1.47-1.44 (m, 9H), 1.93-1.87 (m, 1H), 1.77-1.70 (m, 1H), 1.55-1.50 (m, 1H), 1.36-1.29 (d, J=6.8 Hz, 3H), 1.27-1.23 (m, 5H), 1.14-1.09 (m, 1H), 1.10-1.04 (d, J=6.3 Hz, 1H).

Example 238 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-((2S*,3R*)-3-hydroxybutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-aminobutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralcel OD-H, 5 μm, 250×30 mm, Mobile phase: 5% MeOH+0.3% iPrNH₂, 95% CO₂). MS (ESI): mass calcd. for C₂₄H₃₂F₃N₅O₃S, 527.6; m/z found, 528.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19-8.16 (m, 1H), 7.40-7.31 (m, 1H), 6.64-6.61 (m, 1H), 4.87-4.83 (s, 1H), 4.25-4.14 (m, 2H), 4.05-3.97 (m, 1H), 3.76-3.36 (m, 3H), 2.09-2.02 (m, 1H), 1.47-1.44 (m, 9H), 1.92-1.85 (m, 1H), 1.79-1.69 (m, 1H), 1.53-1.51 (m, 1H), 1.28-1.26 (m, 3H), 1.25-1.23 (m, 4H), 1.12-1.09 (d, J=6.4 Hz, 1H), 1.09-1.06 (d, J=6.2 Hz, 1H).

Example 239 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(3S,4R)-4-hydroxytetrahydrofuran-3-yl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3R,4S)-4-amino-tetrahydro-furan-3-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₄S, 577.6; m/z found, 578.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 7.37-7.27 (m, 1H), 7.03-6.67 (m, 2H), 4.93-4.85 (m, 1H), 4.82-4.71 (s, 1H), 4.47-4.36 (m, 2H), 4.30-4.09 (m, 3H), 3.89-3.74 (m, 2H), 3.62-3.29 (m, 3H), 2.04-1.88 (m, 3H), 1.81-1.52 (m, 3H), 1.24-1.21 (dd, J=6.3, 3.6 Hz, 2H), 1.08-1.02 (m, 3H), 1.00-0.97 (m, 1H).

Example 240 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-(1,1-dioxothietan-3-yl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting 3-aminothietane 1,1-dioxide HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₄S₂, 595.6; m/z found, 596.0 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.01 (m, 1H), 7.87-7.77 (m, 1H), 7.06-6.64 (m, 2H), 4.95-4.72 (m, 3H), 4.68-4.59 (m, 2H), 4.32-4.16 (m, 3H), 3.63-3.32 (m, 2H), 2.12-2.05 (m, 1H), 2.03-1.91 (m, 2H), 1.64-1.52 (m, 2H), 1.24-1.21 (m, 2H), 1.09-1.00 (m, 4H).

Example 241 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpiperidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 108: Step B) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₄F₅N₅O₃S, 591.6; m/z found, 592.2 [M+H]⁺. ¹H NMR (600 MHz, CDCl₃) δ 8.11-8.08 (s, 1H), 7.45-7.38 (m, 1H), 6.94-6.65 (m, 2H), 4.93-4.40 (m, 3H), 4.11-4.05 (m, 1H), 3.94-3.31 (m, 1H), 3.00-2.75 (m, 1H), 2.09-1.94 (m, 2H), 1.67-1.48 (m, 5H), 1.44-1.33 (m, 1H), 1.31-1.27 (m, 9H), 1.19-1.08 (m, 3H), 1.06-1.02 (m, 3H).

Example 242 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.6; m/z found, 590.2 [M+H]⁺. ¹H NMR (600 MHz, CDCl₃) δ 8.09-8.04 (s, 1H), 7.46-7.41 (d, J=9.2 Hz, 1H), 6.90-6.68 (m, 2H), 4.87-4.25 (m, 4H), 4.11-4.05 (m, 1H), 2.00-1.94 (m, 2H), 1.81-1.71 (m, 2H), 1.64-1.52 (m, 3H), 1.48-1.42 (m, 4H), 1.32-1.30 (s, 3H), 1.30-1.28 (m, 6H), 1.06-1.02 (m, 3H).

Example 243 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N—((R*)-2,3-dihydroxy-3-methylbutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 1-amino-3-methyl-2,3-butanediol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 20% iPrOH/EtOH 50/50 v/v+0.5% iPrNH₂, 80% CO₂, second eluting enantiomer). MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₄S, 557.6; m/z found, 558.2 [M+H]⁺. ¹H NMR (600 MHz, CDCl₃) δ 8.19-8.15 (m, 1H), 7.72-7.63 (m, 1H), 6.64-6.60 (m, 1H), 4.89-4.84 (s, 1H), 4.30-4.17 (m, 1H), 3.87-3.81 (m, 1H), 3.64-3.59 (m, 1H), 3.46-3.35 (m, 2H), 1.46-1.44 (m, 9H), 3.13-3.04 (m, 1H), 2.10-1.96 (m, 2H), 1.94-1.72 (m, 2H), 1.55-1.49 (m, 1H), 1.33-1.30 (s, 3H), 1.28-1.26 (s, 3H), 1.23-1.19 (m, 3H), 1.11-1.08 (d, J=6.4 Hz, 1H).

Example 244 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N—((S*)-2,3-dihydroxy-3-methylbutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 243. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 20% iPrOH/EtOH 50/50 v/v+0.5% iPrNH₂, 80% CO₂, first eluting enantiomer). MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₄S, 557.6; m/z found, 558.2 [M+H]⁺. ¹H NMR (600 MHz, CDCl₃) δ 8.18-8.15 (m, 1H), 7.74-7.63 (m, 1H), 6.66-6.59 (m, 1H), 4.92-4.84 (s, 1H), 1.47-1.44 (m, 9H), 4.37-4.17 (m, 1H), 3.88-3.82 (m, 1H), 3.65-3.60 (m, 1H), 3.51-3.46 (m, 1H), 3.42-3.32 (m, 2H), 2.08-2.01 (m, 1H), 1.95-1.87 (m, 1H), 1.77-1.70 (m, 1H), 1.64-1.50 (m, 2H), 1.32-1.29 (s, 3H), 1.27-1.26 (s, 3H), 1.24-1.20 (m, 3H), 1.10-1.06 (d, J=6.4 Hz, 1H).

Example 245 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 109: Step B) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₀F₇N₅O₃S, 613.6; m/z found, 614.2 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.07-8.00 (m, 1H), 7.42-7.34 (m, 1H), 6.94-6.56 (m, 2H), 4.88-4.46 (m, 3H), 4.11-3.77 (m, 3H), 2.66-2.47 (m, 1H), 2.21-2.05 (m, 1H), 2.02-1.94 (m, 1H), 1.93-1.84 (m, 1H), 1.65-1.56 (m, 1H), 1.38-1.34 (d, J=6.4 Hz, 2H), 1.33-1.29 (m, 9H), 1.27-1.25 (m, 1H), 1.08-1.02 (t, J=7.4 Hz, 3H).

Example 246 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1S)-2-hydroxy-1,2-dimethyl-propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 109: Step B) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₀F₇N₅O₃S, 613.6; m/z found, 614.2 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.07-8.01 (m, 1H), 7.39-7.33 (d, J=9.2 Hz, 1H), 6.94-6.56 (m, 2H), 4.84-4.47 (m, 3H), 4.11-3.79 (m, 3H), 2.64-2.48 (m, 1H), 2.21-2.05 (m, 1H), 2.03-1.93 (m, 1H), 1.90-1.79 (m, 1H), 1.38-1.34 (d, J=6.4 Hz, 2H), 1.33-1.30 (m, 9H), 1.30-1.26 (m, 2H), 1.08-1.02 (t, J=7.4 Hz, 3H).

Example 247 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1S)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpiperidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 108: Step B) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₄F₅N₅O₃S, 591.6; m/z found, 592.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12-8.07 (s, 1H), 7.47-7.40 (d, J=9.3 Hz, 1H), 6.98-6.60 (m, 2H), 4.94-4.40 (m, 3H), 4.12-4.05 (m, 1H), 3.94-3.31 (m, 1H), 2.99-2.74 (m, 1H), 2.12-2.05 (m, 1H), 2.02-1.93 (m, 1H), 1.68-1.39 (m, 6H), 1.31-1.27 (m, 9H), 1.21-1.18 (d, J=6.8 Hz, 1H), 1.12-1.01 (m, 5H).

Example 248 4-(1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1S)-2-hydroxy-1,2-dimethyl-propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.6; m/z found, 590.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09-8.05 (s, 1H), 7.48-7.42 (d, J=9.2 Hz, 1H), 6.95-6.64 (m, 2H), 4.92-4.66 (m, 3H), 4.31-4.24 (m, 1H), 4.12-4.05 (m, 1H), 2.03-1.92 (m, 2H), 1.83-1.73 (m, 2H), 1.67-1.51 (m, 3H), 1.49-1.42 (m, 4H), 1.32-1.28 (m, 9H), 1.07-1.01 (m, 3H).

Example 249 [5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-2-[3-(hydroxymethyl)azetidine-1-carbonyl]thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 148 substituting azetidin-3-ylmethanol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₃S, 525.6; m/z found, 526.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.18-8.12 (m, 1H), 6.64-6.59 (m, 1H), 4.94-4.86 (s, 1H), 4.83-4.70 (m, 1H), 4.54-4.45 (m, 1H), 4.34-4.14 (m, 2H), 4.06-3.97 (m, 1H), 3.89-3.83 (m, 2H), 3.61-3.44 (m, 2H), 2.99-2.89 (m, 1H), 2.11-2.02 (m, 2H), 1.95-1.73 (m, 2H), 1.59-1.50 (m, 1H), 1.47-1.43 (s, 9H), 1.24-1.21 (m, 2H), 1.09-0.89 (m, 1H).

Example 250 [5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-2-(3-hydroxyazetidine-1-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 149 substituting 3-hydroxyazetidine HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₈F₃N₅O₃S, 511.6; m/z found, 512.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17-8.11 (m, 1H), 6.65-6.59 (m, 1H), 4.99-4.85 (m, 2H), 4.79-4.69 (m, 1H), 4.55-4.43 (m, 2H), 4.23-4.14 (m, 1H), 4.11-4.05 (m, 1H), 3.61-3.43 (m, 2H), 3.34-3.24 (m, 1H), 2.10-2.02 (m, 1H), 1.97-1.74 (m, 2H), 1.61-1.48 (m, 1H), 1.48-1.41 (s, 9H), 1.24-1.20 (dd, J=6.3, 3.5 Hz, 2H), 1.08-0.90 (dd, J=8.5, 6.5 Hz, 1H).

Example 251 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-((1s,3R)-3-hydroxycyclobutyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-3-amino-cyclobutanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₃S, 525.6; m/z found, 526.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20-8.13 (m, 1H), 7.42-7.28 (m, 1H), 6.66-6.61 (m, 1H), 4.98-4.91 (m, 1H), 4.24-4.09 (m, 3H), 3.63-3.32 (m, 2H), 2.95-2.84 (m, 2H), 1.47-1.41 (m, 9H), 2.52-2.45 (m, 1H), 2.09-2.05 (m, 1H), 2.04-2.00 (m, 1H), 1.94-1.70 (m, 3H), 1.57-1.48 (m, 1H), 1.25-1.22 (d, J=6.3 Hz, 2H), 1.10-1.03 (d, J=6.4 Hz, 1H).

Example 252 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-(cis-2-hydroxycyclopentyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-2-amino-cyclopentanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09-8.00 (m, 1H), 7.63-7.56 (m, 1H), 7.04-6.63 (m, 2H), 4.88-4.70 (m, 2H), 4.39-4.17 (m, 3H), 3.61-3.35 (m, 2H), 2.19-2.06 (m, 2H), 2.01-1.89 (m, 4H), 1.80-1.49 (m, 7H), 1.23-1.19 (m, 2H), 1.09-1.02 (m, 4H).

Example 253 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-(3-methyloxetan-3-yl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

To a microwave vial under N₂ was added ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (100 mg, 0.21 mmol, Intermediate 107), 3-methyl-3-oxetanamine (47.4 μL, 1.03 mmol) and EtOH (0.98 mL), and the reaction was stirred at 100° C. for 21 h. An additional aliquot of 3-methyl-3-oxetanamine (95 μL, 2.06 mmol) was added and the mixture stirred at 100° C. for 6 h. An additional aliquot of 3-methyl-3-oxetanamine (95 μL, 2.06 mmol) was added and the mixture stirred at 100° C. for 17 h. The reaction mixture was cooled to rt and partitioned between EtOAc (20 mL) and saturated aqueous NH₄Cl (20 mL). The layers were separated and the aqueous further extracted with EtOAc (2×15 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-100% EtOAc/Hexanes) to provide the title compound. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₃S, 525.6; m/z found, 526.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.19-8.11 (s, 1H), 7.55-7.43 (m, 1H), 6.65-6.59 (m, 1H), 5.06-4.97 (m, 1H), 4.95-4.88 (m, 2H), 4.58-4.51 (d, J=6.6 Hz, 2H), 4.24-4.13 (m, 1H), 3.60-3.31 (m, 2H), 2.08-1.99 (m, 1H), 1.93-1.82 (m, 2H), 1.77-1.70 (m, 3H), 1.56-1.45 (m, 1H), 1.45-1.41 (s, 9H), 1.22-1.19 (d, J=6.3 Hz, 2H), 1.07-1.02 (d, J=6.4 Hz, 1H).

Example 254 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-(1,1-dioxothian-4-yl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 4-aminotetrahydro-2H-thiopyran 1,1-dioxide for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₄S₂, 587.7; m/z found, 588.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.15-8.06 (s, 1H), 7.41-7.33 (m, 1H), 6.66-6.58 (s, 1H), 5.12-5.05 (s, 1H), 4.29-4.11 (m, 2H), 3.60-3.27 (m, 2H), 3.18-3.08 (m, 4H), 2.44-2.34 (m, 2H), 2.32-2.19 (m, 2H), 2.11-2.02 (m, 1H), 1.91-1.65 (m, 2H), 1.54-1.45 (m, 1H), 1.44-1.38 (s, 9H), 1.21-1.18 (d, J=6.3 Hz, 2H), 1.06-1.00 (d, J=6.4 Hz, 1H).

Example 255 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-N-((3S*,4S*)-4-hydroxytetrahydrofuran-3-yl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 228. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×30 mm, Mobile phase: 25% iPrOH+0.3% iPrNH₂, 75% CO₂, first eluting enantiomer). MS (ESI): mass calcd. for C₂₄H₂₅F₆N₅O₄S, 593.5; m/z found, 594.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.23-8.19 (s, 1H), 7.82-7.77 (d, J=7.8 Hz, 1H), 6.76-6.72 (s, 1H), 4.99-4.89 (m, 2H), 4.69-4.45 (m, 4H), 4.23-4.17 (m, 1H), 4.11-4.05 (dd, J=10.3, 4.4 Hz, 1H), 3.91-3.86 (m, 1H), 3.77-3.71 (m, 1H), 2.25-2.16 (m, 1H), 1.82-1.65 (m, 4H), 1.49-1.40 (m, 7H).

Example 256 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-4-[(2S)-4,4-difluoro-2-methyl-pyrrolidine-1-carbonyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 110) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₃F₄N₅O₃S, 559.6; m/z found, 560.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.03-7.97 (m, 1H), 7.41-7.34 (m, 1H), 6.90-6.53 (m, 2H), 4.90-4.84 (s, 1H), 4.71-4.47 (m, 1H), 4.11-3.81 (m, 3H), 1.48-1.44 (m, 9H), 2.65-2.46 (m, 1H), 2.11-2.05 (m, 1H), 1.99-1.89 (m, 1H), 1.70-1.60 (m, 1H), 1.38-1.34 (d, J=6.4 Hz, 2H), 1.33-1.29 (m, 9H).

Example 257 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-4-[(2S)-4,4-difluoro-2-methyl-pyrrolidine-1-carbonyl]-N-[(1S)-2-hydroxy-1,2-dimethyl-propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 110) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₃F₄N₅O₃S, 559.6; m/z found, 560.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.03-7.98 (m, 1H), 7.40-7.32 (d, J=9.2 Hz, 1H), 6.90-6.53 (m, 2H), 4.90-4.84 (s, 1H), 4.62-4.46 (m, 1H), 4.11-3.77 (m, 3H), 1.70-1.60 (m, 1H), 2.62-2.47 (m, 1H), 2.19-2.05 (m, 1H), 1.98-1.86 (m, 1H), 1.48-1.43 (s, 9H), 1.38-1.34 (d, J=6.5 Hz, 2H), 1.32-1.28 (m, 9H).

Example 258 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-((1r,3S)-3-hydroxycyclobutyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-3-aminocyclobutanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₃S, 525.6; m/z found, 526.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20-8.14 (s, 1H), 7.38-7.28 (m, 1H), 6.65-6.60 (m, 1H), 4.96-4.91 (m, 1H), 4.71-4.55 (m, 2H), 4.24-4.10 (m, 1H), 3.64-3.33 (m, 2H), 2.51-2.39 (m, 4H), 2.18-2.13 (m, 1H), 2.10-1.70 (m, 3H), 1.57-1.49 (m, 1H), 1.47-1.42 (s, 9H), 1.25-1.22 (d, J=6.3 Hz, 2H), 1.09-1.03 (d, J=6.4 Hz, 1H).

Example 259 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-N-(oxetan-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-oxetanamine for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₈F₃N₅O₃S, 511.6; m/z found, 512.1 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.20-8.15 (s, 1H), 7.76-7.62 (m, 1H), 6.66-6.59 (m, 1H), 5.30-5.20 (m, 1H), 5.04-4.97 (m, 2H), 4.94-4.87 (s, 1H), 4.71-4.64 (m, 2H), 4.26-4.16 (m, 1H), 3.65-3.32 (m, 2H), 2.12-2.04 (m, 1H), 1.96-1.72 (m, 2H), 1.58-1.48 (m, 1H), 1.47-1.43 (s, 9H), 1.26-1.24 (d, J=6.4 Hz, 2H), 1.10-1.04 (d, J=6.4 Hz, 1H).

Example 260 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-(1,1-dioxothietan-3-yl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

To a microwave vial under N₂ was added ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (100 mg, 0.21 mmol, Intermediate 107), 3-aminothietane 1,1-dioxide HCl (171 mg, 1.03 mmol), DIPEA (196 μL, 1.14 mmol) and EtOH (0.98 mL), and the reaction was stirred at 100° C. for 18 h. An additional aliquot of DIPEA (500 μL, 2.91 mmol) was added and the mixture stirred at 100° C. for 6 h. An additional aliquot of 3-aminothietane 1,1-dioxide HCl (171 mg, 1.03 mmol) was added and the mixture stirred at 100° C. for 17 h. The reaction mixture was cooled to rt and partitioned between EtOAc (20 mL) and saturated aqueous NH₄Cl (20 mL). The layers were separated and the aqueous further extracted with EtOAc (2×15 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated to dryness. The crude residue was dissolved in DCM and purified by FCC (0-100% EtOAc/Hexanes) to provide the title compound. MS (ESI): mass calcd. for C₂₃H₂₈F₃N₅O₄S₂, 559.6; m/z found, 560.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.19-8.12 (s, 1H), 7.99-7.91 (m, 1H), 6.67-6.60 (m, 1H), 4.95-4.91 (s, 1H), 4.91-4.83 (m, 1H), 4.65-4.54 (m, 2H), 4.25-4.15 (m, 3H), 3.66-3.31 (m, 2H), 2.11-2.03 (m, 1H), 1.96-1.71 (m, 2H), 1.59-1.50 (m, 1H), 1.49-1.43 (s, 9H), 1.26-1.24 (m, 2H), 1.11-1.05 (d, J=6.4 Hz, 1H).

Example 261 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[3-(hydroxymethyl)oxetan-3-yl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3-aminooxetan-3-yl)methanol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₄S, 541.6; m/z found, 542.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17-8.14 (s, 1H), 7.84-7.74 (m, 1H), 6.65-6.61 (m, 1H), 4.98-4.93 (s, 1H), 4.91-4.85 (m, 2H), 4.69-4.65 (m, 2H), 4.22-4.14 (m, 3H), 1.77-1.73 (m, 1H), 3.57-3.20 (m, 3H), 2.10-2.04 (m, 1H), 1.91-1.85 (m, 1H), 1.56-1.47 (m, 1H), 1.47-1.44 (s, 9H), 1.24-1.21 (d, J=6.3 Hz, 2H), 1.09-1.05 (d, J=6.4 Hz, 1H).

Example 262 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[1-(hydroxymethyl)cyclobutyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (1-aminocyclobutyl)methanol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.20-8.14 (s, 1H), 7.56-7.47 (m, 1H), 6.65-6.59 (m, 1H), 4.97-4.90 (s, 1H), 4.24-4.16 (m, 1H), 3.94-3.89 (d, J=5.8 Hz, 2H), 3.62-3.34 (m, 3H), 2.37-2.30 (m, 4H), 2.03-1.98 (m, 1H), 1.94-1.86 (m, 2H), 1.78-1.71 (m, 1H), 1.57-1.49 (m, 1H), 1.47-1.44 (s, 9H), 1.24-1.22 (d, J=6.3 Hz, 2H), 1.12-1.07 (d, J=6.4 Hz, 1H).

Example 263 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[1-(hydroxymethyl)cyclopropyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 1-amino-cyclopropanemethanol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₃S, 525.6; m/z found, 526.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.18-8.14 (s, 1H), 7.70-7.58 (m, 1H), 6.66-6.61 (m, 1H), 4.97-4.91 (s, 1H), 4.23-4.15 (m, 1H), 3.77-3.69 (m, 2H), 3.60-3.32 (m, 3H), 2.09-2.05 (m, 1H), 1.93-1.85 (m, 1H), 1.77-1.73 (m, 1H), 1.55-1.48 (m, 1H), 1.47-1.44 (s, 9H), 1.24-1.21 (d, J=6.3 Hz, 2H), 1.06-1.03 (d, J=6.4 Hz, 1H), 1.03-1.00 (s, 4H).

Example 264 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-N-[3,3,3-trifluoro-2-hydroxy-2-(trifluoromethyl)propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 2-(aminomethyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (Intermediate 111) for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₄H₂₇F₈N₅O₃S, 617.6; m/z found, 618.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.04-7.96 (m, 1H), 7.84-7.72 (m, 1H), 6.93-6.49 (m, 3H), 4.94-4.87 (s, 1H), 4.26-4.15 (m, 1H), 4.09-3.99 (m, 2H), 1.47-1.44 (m, 9H), 3.61-3.28 (m, 2H), 2.10-2.05 (m, 1H), 1.97-1.73 (m, 2H), 1.59-1.50 (m, 1H), 1.24-1.21 (d, J=6.3 Hz, 2H), 1.02-0.99 (d, J=6.4 Hz, 1H).

Example 265 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-(2-hydroxy-2-methyl-propyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 59) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₃₃F₂N₅O₃S, 509.6; m/z found, 510.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.05-7.98 (m, 1H), 7.66-7.54 (m, 1H), 7.00-6.61 (m, 2H), 4.89 (s, 1H), 4.30-4.18 (m, 1H), 3.60-3.32 (m, 4H), 2.97-2.87 (m, 1H), 1.47-1.44 (m, 9H), 2.36-2.22 (m, 1H), 1.93-1.85 (m, 1H), 1.79-1.49 (m, 2H), 1.31 (s, 6H), 1.23 (d, J=6.3 Hz, 2H), 1.02 (d, J=6.4 Hz, 1H).

Example 266 N-(1,1-Dideuterio-2-hydroxy-2-methyl-propyl)-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting 1-amino-2-methylpropan-1,1-d₂-2-ol HCl (Intermediate 76: Step C) for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈D₂F₅N₅O₃S, 565.6; m/z found, 566.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.61-7.50 (m, 1H), 7.04-6.64 (m, 2H), 4.91-4.70 (m, 2H), 4.39-4.16 (m, 1H), 3.60-3.38 (m, 2H), 2.14-2.05 (m, 1H), 2.03-1.84 (m, 3H), 1.82-1.73 (m, 1H), 1.66-1.51 (m, 2H), 1.31 (s, 6H), 1.23-1.20 (m, 2H), 1.08-1.02 (m, 4H).

Example 267 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₅N₅O₃S, 577.6; m/z found, 578.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 7.44-7.37 (m, 1H), 7.04-6.65 (m, 2H), 4.85-4.71 (m, 2H), 4.38-4.16 (m, 1H), 4.12-4.06 (m, 1H), 3.64-3.35 (m, 2H), 2.04-1.87 (m, 4H), 1.82-1.72 (m, 1H), 1.64-1.48 (m, 2H), 1.32-1.28 (m, 9H), 1.23-1.20 (m, 2H), 1.08-1.02 (m, 4H).

Example 268 [5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-2-(3-hydroxy-3-methyl-azetidine-1-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 149 substituting 3-hydroxy-3-methylazetidine HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₃S, 525.6; m/z found, 526.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.18-8.12 (m, 1H), 6.64-6.60 (m, 1H), 4.97-4.90 (m, 1H), 4.65-4.52 (m, 2H), 4.22-4.09 (m, 3H), 3.61-3.42 (m, 2H), 2.95-2.84 (m, 1H), 2.11-2.04 (m, 1H), 1.97-1.72 (m, 2H), 1.61-1.57 (m, 3H), 1.57-1.50 (m, 1H), 1.45 (s, 9H), 1.24-1.20 (m, 2H), 1.09-1.00 (m, 1H).

Example 269 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₅H₃₅F₂N₅O₃S, 523.6; m/z found, 524.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.06-7.97 (m, 1H), 7.44-7.35 (m, 1H), 7.01-6.60 (m, 2H), 4.87 (s, 1H), 4.31-4.17 (m, 1H), 4.10-4.03 (m, 1H), 3.64-3.29 (m, 2H), 2.11-2.05 (m, 1H), 2.02-1.85 (m, 2H), 1.80-1.73 (m, 1H), 1.58-1.49 (m, 1H), 1.46 (s, 9H), 1.31-1.27 (m, 9H), 1.24-1.21 (m, 2H), 1.04 (d, J=6.4 Hz, 1H).

Example 270 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1S)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₅H₃₅F₂N₅O₃S, 523.6; m/z found, 524.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.05-7.98 (m, 1H), 7.43-7.36 (m, 1H), 7.00-6.60 (m, 2H), 4.87 (s, 1H), 4.27-4.17 (m, 1H), 4.11-4.05 (m, 1H), 3.63-3.32 (m, 2H), 1.47-1.44 (m, 9H), 2.09-2.05 (m, 1H), 2.00-1.84 (m, 2H), 1.79-1.72 (m, 1H), 1.57-1.49 (m, 1H), 1.31-1.28 (m, 9H), 1.22 (d, J=6.3 Hz, 2H), 1.05 (d, J=6.4 Hz, 1H).

Example 271 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-N-[3,3,3-trifluoro-2-hydroxy-2-(trifluoromethyl)propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 2-(aminomethyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (Intermediate 111) for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₆F₉N₅O₃S, 635.5; m/z found, 636.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.15-8.11 (m, 1H), 7.90-7.81 (m, 1H), 6.64 (s, 1H), 6.52 (s, 1H), 4.95 (s, 1H), 4.24-4.16 (m, 1H), 1.48-1.44 (m, 9H), 4.08-3.95 (m, 2H), 3.61-3.29 (m, 2H), 1.94-1.71 (m, 2H), 1.59-1.50 (m, 1H), 1.28-1.23 (m, 3H), 1.08 (d, J=6.4 Hz, 1H).

Example 272 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1S)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₅N₅O₃S, 577.6; m/z found, 578.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.45-7.34 (m, 1H), 7.04-6.64 (m, 2H), 4.88-4.71 (m, 2H), 4.30-4.06 (m, 2H), 3.64-3.34 (m, 2H), 2.04-1.84 (m, 4H), 1.83-1.71 (m, 1H), 1.64-1.50 (m, 2H), 1.33-1.27 (m, 9H), 1.24-1.19 (m, 2H), 1.10-1.01 (m, 4H).

Example 273 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[1-(trifluoromethyl)cyclobutyl]methylamino]-3-pyridyl]-N-(2-hydroxy-2-methyl-propyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-4-(difluoromethyl)-N-((1-(trifluoromethyl)cyclobutyl)methyl)pyridin-2-amine (Intermediate 112) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₀F₇N₅O₃S, 625.6; m/z found, 626.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.07-8.02 (m, 1H), 7.58-7.47 (m, 1H), 6.93-6.53 (m, 2H), 5.04-4.93 (m, 1H), 4.77-4.45 (m, 1H), 4.14-3.86 (m, 2H), 3.86-3.80 (m, 2H), 3.58-3.41 (m, 2H), 2.64-2.48 (m, 1H), 2.40-2.29 (m, 2H), 2.15-1.96 (m, 6H), 1.36 (d, J=6.4 Hz, 2H), 1.35-1.31 (m, 6H), 1.23 (d, J=6.4 Hz, 1H).

Example 274 5-[4-(Difluoromethyl)-6-[[1-(trifluoromethyl)cyclobutyl]methylamino]-3-pyridyl]-N-(2-hydroxy-2-methyl-propyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-4-(difluoromethyl)-N-((1-(trifluoromethyl)cyclobutyl)methyl)pyridin-2-amine (Intermediate 112) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.6; m/z found, 590.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 7.62-7.51 (m, 1H), 7.03-6.62 (m, 2H), 5.01-4.93 (m, 1H), 4.37-4.17 (m, 1H), 3.87-3.80 (m, 2H), 3.61-3.37 (m, 4H), 2.39-2.27 (m, 2H), 2.08-2.06 (m, 1H), 2.04-1.95 (m, 4H), 1.94-1.72 (m, 2H), 1.59-1.50 (m, 1H), 1.32 (s, 6H), 1.23 (d, J=6.3 Hz, 2H), 1.04 (d, J=6.4 Hz, 1H).

Example 275 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[1-(trifluoromethyl)cyclopropyl]methylamino]-3-pyridyl]-N-(2-hydroxy-2-methyl-propyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-4-(difluoromethyl)-N-((1-(trifluoromethyl)cyclopropyl)methyl)pyridin-2-amine (Intermediate 113) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₂₈F₇N₅O₃S, 611.6; m/z found, 612.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.01 (s, 1H), 7.55-7.45 (m, 1H), 6.88-6.55 (m, 2H), 5.11-5.05 (m, 1H), 4.74-4.46 (m, 1H), 4.11-3.80 (m, 2H), 3.68 (d, J=5.7 Hz, 2H), 3.56-3.40 (m, 2H), 2.65-2.48 (m, 1H), 2.19-2.06 (m, 1H), 1.98-1.86 (m, 1H), 1.36 (d, J=6.4 Hz, 2H), 1.34-1.31 (m, 6H), 1.23 (d, J=6.6 Hz, 1H), 1.09-1.03 (m, 2H), 0.90-0.84 (m, 2H).

Example 276 5-[4-(Difluoromethyl)-6-[[1-(trifluoromethyl)cyclopropyl]methylamino]-3-pyridyl]-N-(2-hydroxy-2-methyl-propyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-4-(difluoromethyl)-N-((1-(trifluoromethyl)cyclopropyl)methyl)pyridin-2-amine (Intermediate 113) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.05-7.98 (m, 1H), 7.60-7.50 (m, 1H), 6.98-6.65 (m, 2H), 5.09-5.02 (m, 1H), 4.36-4.16 (m, 1H), 3.71-3.65 (m, 2H), 3.58-3.37 (m, 4H), 2.04-2.00 (m, 1H), 1.95-1.74 (m, 2H), 1.58-1.51 (m, 1H), 1.32 (s, 6H), 1.23 (d, J=6.3 Hz, 2H), 1.08-1.01 (m, 3H), 0.89-0.84 (m, 2H).

Example 277 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-N-(2-hydroxy-2-methyl-propyl)-5-[6-[(1-methylcyclopropyl)methylamino]-4-(trifluoromethyl)-3-pyridyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-((1-methylcyclopropyl)methyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 114) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide (Intermediate 67) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.14 (s, 1H), 7.56-7.45 (m, 1H), 6.65 (s, 1H), 5.13-5.05 (m, 1H), 4.75-4.43 (m, 1H), 4.14-3.75 (m, 2H), 3.56-3.42 (m, 2H), 3.20 (d, J=5.0 Hz, 2H), 2.62-2.48 (m, 1H), 2.19-2.01 (m, 1H), 1.98-1.83 (m, 1H), 1.36 (d, J=6.4 Hz, 2H), 1.34-1.31 (m, 6H), 1.31-1.27 (m, 1H), 1.16 (s, 3H), 0.51-0.47 (m, 2H), 0.42-0.38 (m, 2H).

Example 278 N-(2-Hydroxy-2-methyl-propyl)-5-[6-[(1-methylcyclopropyl)methylamino]-4-(trifluoromethyl)-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-((1-methylcyclopropyl)methyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 114) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.17 (s, 1H), 7.62-7.53 (m, 1H), 6.66-6.59 (m, 1H), 5.17-5.05 (m, 1H), 4.36-4.14 (m, 1H), 3.61-3.40 (m, 4H), 3.24-3.15 (m, 2H), 2.11-1.86 (m, 3H), 1.80-1.69 (m, 1H), 1.58-1.49 (m, 1H), 1.34-1.28 (m, 6H), 1.25-1.23 (m, 2H), 1.16 (s, 3H), 1.13-1.09 (m, 1H), 0.51-0.46 (m, 2H), 0.41-0.35 (m, 2H).

Example 279 5-(6-(((S*)-2,2-Difluorocyclopentyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-N-(2,2-difluorocyclopentyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 64: Step B) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×20 mm, Mobile phase: 15% EtOH/iPrOH 50/50 v/v+0.3% iPrNH₂, 85% CO₂, second eluting enantiomer). MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.21 (s, 1H), 7.59-7.49 (m, 1H), 6.76 (s, 1H), 5.22-5.08 (m, 1H), 4.58-4.45 (m, 1H), 4.38-4.17 (m, 1H), 3.55-3.41 (m, 4H), 2.09-2.02 (m, 1H), 2.40-2.32 (m, 1H), 2.28-2.16 (m, 2H), 1.91-1.72 (m, 4H), 1.66-1.55 (m, 3H), 1.32 (s, 6H), 1.24 (d, J=6.3 Hz, 2H), 1.21-1.13 (m, 1H).

Example 280 5-(6-(((R*)-2,2-Difluorocyclopentyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 279. The pure diastereomer was isolated via SFC (Stationary phase: Chiralpak AD-H, 5 μm, 250×20 mm, Mobile phase: 15% EtOH/iPrOH 50/50 v/v+0.3% iPrNH₂, 85% CO₂, first eluting enantiomer). MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.21 (s, 1H), 7.61-7.51 (m, 1H), 6.76-6.70 (m, 1H), 5.19-5.10 (m, 1H), 4.63-4.50 (m, 1H), 4.38-4.15 (m, 1H), 3.58-3.39 (m, 4H), 2.39-2.30 (m, 1H), 2.28-2.13 (m, 2H), 2.10-2.02 (m, 1H), 1.94-1.72 (m, 4H), 1.61-1.52 (m, 3H), 1.33-1.30 (m, 6H), 1.25 (d, J=6.2 Hz, 2H), 1.22-1.09 (m, 1H).

Example 281 5-[5-Cyano-6-(cyclohexylamino)-3-pyridyl]-N-(2-hydroxy-2-methyl-propyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting 5-bromo-2-(cyclohexylamino)nicotinonitrile (Intermediate 9) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₆H₃₄N₆O₃S, 510.7; m/z found, 511.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.43 (d, J=2.5 Hz, 1H), 7.92-7.88 (m, 1H), 7.63-7.54 (m, 1H), 5.29-5.23 (m, 1H), 4.39-3.96 (m, 2H), 3.72-3.21 (m, 4H), 2.39-2.30 (m, 1H), 2.12-2.06 (m, 1H), 2.03-1.98 (m, 1H), 1.94-1.86 (m, 1H), 1.82-1.75 (m, 3H), 1.70-1.65 (m, 1H), 1.64-1.57 (m, 1H), 1.47-1.38 (m, 2H), 1.35 (d, J=6.4 Hz, 2H), 1.31-1.29 (m, 6H), 1.28-1.25 (m, 2H), 0.93 (d, J=6.4 Hz, 1H).

Example 282 N-(2-Hydroxy-2-methyl-propyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-5-[4-(trifluoromethyl)-6-[[(1R)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 77 substituting (R)-5-bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 115) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine. MS (ESI): mass calcd. for C₂₄H₂₉F₆N₅O₃S, 581.6; m/z found, 582.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.24-8.19 (m, 1H), 7.62-7.52 (m, 1H), 6.79-6.74 (m, 1H), 4.92-4.84 (m, 1H), 4.78 (s, 1H), 4.40-4.16 (m, 1H), 3.59-3.43 (m, 4H), 2.07-1.90 (m, 4H), 1.81-1.72 (m, 1H), 1.67-1.63 (m, 1H), 1.58-1.51 (m, 1H), 1.32 (s, 6H), 1.23 (d, J=6.2 Hz, 2H), 1.15 (d, J=6.4 Hz, 1H), 1.08-1.01 (m, 3H).

Example 283 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1R,2R)-2-hydroxycyclopentyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (1R,2R)-trans-2-aminocyclopentanol HCl for 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.2; m/z found, 562.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.12-8.04 (m, 1H), 7.25-7.18 (m, 1H), 7.00-6.66 (m, 2H), 5.00-4.89 (m, 1H), 4.83-4.76 (m, 1H), 4.27-4.13 (m, 2H), 4.08-4.01 (m, 1H), 3.78-3.73 (m, 1H), 3.62-3.31 (m, 2H), 2.32-2.24 (m, 1H), 2.15-1.69 (m, 7H), 1.67-1.50 (m, 2H), 1.42 (d, J=6.9 Hz, 3H), 1.25-1.00 (m, 3H).

Example 284 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N—((R)-1-hydroxypropan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₂H₂₆F₅N₅O₃S, 535.2; m/z found, 536.2 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.11-8.03 (m, 1H), 7.30-7.27 (m, 1H), 7.00-6.65 (m, 2H), 5.00-4.89 (m, 1H), 4.83-4.76 (m, 1H), 4.33-4.17 (m, 2H), 3.84-3.77 (m, 1H), 3.73-3.66 (m, 1H), 3.62-3.34 (m, 2H), 2.28-2.23 (m, 1H), 2.09-1.99 (m, 1H), 1.97-1.86 (m, 1H), 1.82-1.62 (m, 1H), 1.59-1.50 (m, 1H), 1.42 (d, J=6.9 Hz, 3H), 1.34 (d, J=6.9 Hz, 3H), 1.24-1.02 (m, 3H).

Example 285 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1S,2S)-2-hydroxycyclopentyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (1S,2S)-2-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.2; m/z found, 562.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.12-8.04 (m, 1H), 7.25-7.17 (m, 1H), 7.01-6.66 (m, 2H), 5.00-4.89 (m, 1H), 4.82-4.75 (m, 1H), 4.27-4.13 (m, 2H), 4.08-4.01 (m, 1H), 3.76 (d, J=2.1 Hz, 1H), 3.62-3.31 (m, 2H), 2.34-2.24 (m, 1H), 2.15-1.70 (m, 7H), 1.68-1.50 (m, 2H), 1.42 (d, J=6.9 Hz, 3H), 1.24-0.99 (m, 3H).

Example 286 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl-1,1-d₂)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and 1-amino-2-methylpropan-1,1-d₂-2-ol HCl (Intermediate 76: Step C) for 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₃H₂₆D₂F₅N₅O₃S, 551.2; m/z found, 552.3 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.13-8.02 (m, 1H), 7.57-7.49 (m, 1H), 7.02-6.66 (m, 2H), 5.00-4.88 (m, 1H), 4.82-4.74 (m, 1H), 4.41-4.16 (m, 1H), 3.65-3.35 (m, 2H), 2.10-1.97 (m, 1H), 1.97-1.73 (m, 3H), 1.70-1.51 (m, 1H), 1.42 (d, J=6.9 Hz, 3H), 1.33-1.30 (m, 6H), 1.25-1.03 (m, 3H).

Example 287 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-N-(tetrahydro-2H-pyran-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and tetrahydro-2H-pyran-4-amine for (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.2; m/z found, 562.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.11-8.03 (m, 1H), 7.10-6.98 (m, 1H), 6.91-6.66 (m, 2H), 5.01-4.89 (m, 1H), 4.80-4.75 (m, 1H), 4.29-4.13 (m, 2H), 4.02 (d, J=11.9 Hz, 2H), 3.63-3.32 (m, 4H), 2.10-1.98 (m, 3H), 1.96-1.71 (m, 2H), 1.70-1.60 (m, 2H), 1.58-1.50 (m, 1H), 1.44-1.39 (m, 3H), 1.24-1.01 (m, 3H).

Example 288 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1S,3S)-3-hydroxycyclopentyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (1S,3S)-3-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.2; m/z found, 562.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12-8.02 (m, 1H), 7.15-6.62 (m, 3H), 5.01-4.88 (m, 1H), 4.85-4.79 (m, 1H), 4.70-4.58 (m, 1H), 4.55-4.46 (m, 1H), 4.29-4.15 (m, 1H), 3.61-3.29 (m, 2H), 2.44-2.32 (m, 1H), 2.25-1.53 (m, 9H), 1.51-1.48 (m, 1H), 1.42 (d, J=6.8 Hz, 3H), 1.24-0.98 (m, 3H).

Example 289 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1R,3R)-3-hydroxycyclopentyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (1R,3R)-3-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.2; m/z found, 562.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.13-8.00 (m, 1H), 7.15-6.61 (m, 3H), 5.01-4.90 (m, 1H), 4.90-4.80 (m, 1H), 4.70-4.58 (m, 1H), 4.54-4.46 (m, 1H), 4.28-4.15 (m, 1H), 3.60-3.30 (m, 2H), 2.43-2.32 (m, 1H), 2.25-1.48 (m, 10H), 1.42 (d, J=6.8 Hz, 3H), 1.25-0.98 (m, 3H).

Example 290 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-(-trans-2-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 117) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. For C₂₄H₂₆F₅N₅O₃S, 559.2; m/z found, 560.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09 (s, 1H), 7.37 (d, J=4.8 Hz, 1H), 6.89-6.64 (m, 2H), 4.99-4.89 (m, 1H), 4.74 (d, J=9.5 Hz, 1H), 4.71-4.64 (m, 1H), 4.25-4.02 (m, 3H), 3.08 (dd, J=3.5, 1.3 Hz, 1H), 2.28-2.15 (m, 2H), 1.82-1.72 (m, 3H), 1.58-1.49 (m, 3H), 1.48-1.40 (m, 7H).

Example 291 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1R*,2R*)-2-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 117) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.1 mm, Mobile phase: 25% iPrOH+0.3% iPrNH₂, 75% CO₂) of Example 290. MS (ESI): mass calcd. for C₂₄H₂₆F₅N₅O₃S, 559.2; m/z found, 560.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09 (s, 1H), 7.39 (d, J=4.9 Hz, 1H), 6.93-6.62 (m, 2H), 5.01-4.90 (m, 1H), 4.81-4.74 (m, 1H), 4.71-4.65 (m, 1H), 4.25-4.01 (m, 3H), 3.13 (s, 1H), 2.29-2.14 (m, 2H), 1.84-1.71 (m, 3H), 1.55-1.50 (m, 3H), 1.49-1.40 (m, 7H).

Example 292 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 117) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.1 mm, Mobile phase: 25% iPrOH+0.3% iPrNH₂, 75% CO₂) of Example 290. MS (ESI): mass calcd. for C₂₄H₂₆F₅N₅O₃S, 559.2; m/z found, 560.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09 (s, 1H), 7.39 (d, J=4.9 Hz, 1H), 6.92-6.61 (m, 2H), 5.02-4.89 (m, 1H), 4.83-4.77 (m, 1H), 4.70-4.64 (m, 1H), 4.27-4.01 (m, 3H), 3.16 (s, 1H), 2.29-2.14 (m, 2H), 1.83-1.70 (m, 3H), 1.57-1.50 (m, 3H), 1.50-1.40 (m, 7H).

Example 293 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1S,2S)-2-hydroxycyclopentyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1S,2S)-2-aminocylclopentanol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 117) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂H₂₈F₅N₅O₃S, 573.2; m/z found, 574.2 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.09 (s, 1H), 7.27-7.24 (m, 1H), 6.89-6.64 (m, 2H), 4.99-4.90 (m, 1H), 4.79 (d, J=9.5 Hz, 1H), 4.71-4.64 (m, 1H), 4.24-4.00 (m, 3H), 3.74-3.69 (m, 1H), 2.32-2.24 (m, 1H), 2.14-2.05 (m, 1H), 1.94-1.69 (m, 5H), 1.66-1.49 (m, 3H), 1.48-1.39 (m, 7H).

Example 294 5-(6-((1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-difluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71, using 5-bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 118, Step B) in place of 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) in place of (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S 575.2 m/z, found 576.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.49-8.36 (m, 1H), 8.04 (s, 1H), 7.86 (d, J=9.0 Hz, 1H), 7.16-6.80 (m, 2H), 4.72-4.65 (m, 1H), 4.56-4.42 (m, 1H), 4.32-3.97 (m, 1H), 3.46-3.36 (m, 2H), 3.29-3.19 (m, 2H), 1.99-1.42 (m, 4H), 1.20-1.14 (m, 1H), 1.11 (s, 6H), 1.07 (d, J=6.2 Hz, 2H), 0.98-0.90 (m, 1H), 0.70-0.60 (m, 1H), 0.57-0.44 (m, 2H), 0.39-0.28 (m, 1H).

Example 295 5-(6-(((S)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-difluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71, using (S)-5-bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 119) in place of 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) in place of (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S 575.2 m/z, found 576.0 [M+H]⁺. ¹HNMR (400 MHz, DMSO-d₆) δ 8.50-8.36 (m, 1H), 8.03 (s, 1H), 7.86 (d, J=9.0 Hz, 1H), 7.22-6.82 (m, 2H), 4.73-4.64 (m, 1H), 4.57-4.42 (m, 1H), 4.32-3.96 (m, 1H), 3.44-3.36 (m, 2H), 3.29-3.18 (m, 2H), 2.02-1.40 (m, 4H), 1.20-1.03 (m, 9H), 0.94 (d, J=6.4 Hz, 1H), 0.70-0.59 (m, 1H), 0.58-0.43 (m, 2H), 0.40-0.26 (m, 1H).

Example 296 (S)-5-(4-Difluoromethyl)-6-((4,4,4-trifluoro-2-methylbutan-2-yl)amino)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71, using 5-bromo-4-(difluoromethyl)-N-(4,4,4-trifluoro-2-methylbutan-2-yl)pyridin-2-amine (Intermediate 120) in place of 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) in place of (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₂F₅N₅O₃S 577.2 m/z, found 578.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.47-8.35 (m, 1H), 8.03-7.97 (m, 1H), 7.28-7.22 (m, 1H), 7.13-6.79 (m, 2H), 4.70-4.65 (m, 1H), 4.21-3.95 (m, 1H), 3.43-3.33 (m, 1H), 3.28-3.18 (m, 3H), 3.12-2.93 (m, 2H), 1.97-1.58 (m, 3H), 1.52-1.32 (m, 7H), 1.10 (s, 6H), 1.07-0.87 (m, 3H).

Example 297 5-(4-(Difluoromethyl)-6-(((R)-3-methylbutan-2-yl)amino)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71, using (R)-5-bromo-4-(difluoromethyl)-N-(3-methylbutan-2-yl)pyridin-2-amine (Intermediate 121) in place of 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) in place of (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₅F₂N₅O₃S 523.2 m/z, found 524.1 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.19-8.03 (m, 1H), 7.98 (s, 1H), 7.05-6.69 (m, 3H), 4.46 (s, 1H), 4.29-3.99 (m, 1H), 3.97-3.87 (m, 1H), 3.52-3.23 (m, 4H), 2.02-1.41 (m, 5H), 1.14 (s, 6H), 1.11-0.94 (m, 6H), 0.93-0.85 (m, 6H).

Example 298 5-(4-(Difluoromethyl)-6-(((R)-3,3-dimethylbutan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71, using (R)-5-bromo-4-(difluoromethyl)-N-(3,3-dimethylbutan-2-yl)pyridin-2-amine (Intermediate 122) in place of 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) in place of (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₇F₂N₅O₃S 537.3 m/z, found 538.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆, t=80° C.) δ 8.19-8.02 (m, 1H), 7.97 (s, 1H), 7.07-6.64 (m, 3H), 4.45 (s, 1H), 4.22-3.99 (m, 2H), 3.48-3.23 (m, 4H), 2.02-1.35 (m, 4H), 1.14 (s, 6H), 1.11-0.94 (m, 6H), 0.92 (s, 9H).

Example 299 5-(4-(Difluoromethyl)-6-(((S)-3,3-dimethylbutan-2-yl)amino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71, using (S)-5-bromo-4-(difluoromethyl)-N-(3,3-dimethylbutan-2-yl)pyridin-2-amine (Intermediate 123) in place of 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) in place of (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₆H₃₇F₂N₅O₃S 537.3 m/z, found 538.3 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.42-8.31 (m, 1H), 7.94 (s, 1H), 7.12-6.76 (m, 3H), 4.68-4.63 (m, 1H), 4.20-3.95 (m, 2H), 3.43-3.32 (m, 1H), 3.29-3.19 (m, 3H), 2.00-1.38 (m, 4H), 1.16-0.96 (m, 12H), 0.89 (s, 9H).

Example 300 5-(4-(Difluoromethyl)-6-(((S)-3-methylbutan-2-yl)amino)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71, using (S)-5-bromo-4-(difluoromethyl)-N-(3-methylbutan-2-yl)pyridin-2-amine (Intermediate 124) in place of 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) in place of (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₅F₂N₅O₃S 523.2 m/z, found 524.1 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.46-8.33 (m, 1H), 7.96 (s, 1H), 7.20-6.73 (m, 3H), 4.72-4.64 (m, 1H), 4.23-3.97 (m, 1H), 3.95-3.82 (m, 1H), 3.49-3.37 (m, 2H), 3.28-3.17 (m, 2H), 2.04-1.36 (m, 5H), 1.18-1.00 (m, 12H), 0.93-0.84 (m, 6H).

Example 301 (S)-5-(6-((Cyclobutylmethyl)amino)-4-(difluoromethyl)pyridine-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 71, using 5-bromo-N-(cyclobutylmethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 125) in place of 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 69) in place of (S)—N-((1-hydroxycyclobutyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S 521.2 m/z, found 522.1 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.43-8.31 (m, 1H), 7.97 (s, 1H), 7.34-7.26 (m, 1H), 7.12-6.76 (m, 1H), 6.73 (s, 1H), 4.71-4.64 (m, 1H), 4.22-3.95 (m, 1H), 3.31-3.15 (m, 6H), 2.57-2.52 (m, 1H), 2.05-1.90 (m, 3H), 1.87-1.77 (m, 3H), 1.74-1.60 (m, 3H), 1.58-1.40 (m, 1H), 1.14-0.88 (m, 9H).

Example 302 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)-N-((5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)methyl)thiazole-2-carboxamide

1,1′-Carbonyldiimidazole (14 mg, 0.087 mmol) was added to a solution of (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylic acid (40 mg, 0.079 mmol, Intermediate 126) in DMF (0.3 mL), and the solution was maintained at rt for 1.5 h. After this time, 5-(aminomethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one hydrochloride (14 mg, 0.095 mmol) and then DIPEA (0.016 mL, 0.095 mmol) were added, and the mixture was stirred at rt for 1 h. The mixture was then diluted with MeOH, filtered, and purified by preparative HPLC (XBridge C18, MeCN/water, 0.05% TFA) to afford the title compound. MS (ESI): mass calcd. for C₂₃H₂₇F₃N₈O₃S, 552.2; m/z found, 552.8 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆, mixture of rotamers) δ 11.37-11.22 (m, 2H of both rotamers), 9.24 (t, J=6.1 Hz, 1H of major rotamer), 9.19 (t, J=6.2 Hz, 1H of minor rotamer), 8.05 (s, 1H of both rotamers), 7.22 (s, 1H of both rotamers), 6.94 (s, 1H of both rotamers), 4.50-4.40 (m, 1H of minor rotamer), 4.38-4.22 (m, 2H of both rotamers), 4.07-3.97 (m, 1H of major rotamer), 3.58-3.50 (m, 1H of both rotamers), 3.43-3.32 (m, 1H of both rotamers), 2.02-1.45 (m, 4H of both rotamers), 1.41 (s, 9H of both rotamers), 1.10 (d, J=6.3 Hz, 3H of major rotamer), 0.94 (d, J=6.4 Hz, 3H of minor rotamer).

Example 303 (S)—N-((1H-Tetrazol-5-yl)methyl)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 302, substituting 1H-1,2,3,4-tetrazol-5-ylmethanamine for 5-(aminomethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one hydrochloride. MS (ESI): mass calcd. for C₂₂H₂₆F₃N₉₀₂S, 537.2; m/z found, 538.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆, tetrazole proton not observed) δ 9.60 (t, J=6.0 Hz, 1H of major rotamer), 9.55 (t, J=6.0 Hz, 1H of minor rotamer), 8.06 (s, 1H of major rotamer), 8.06 (s, 1H of minor rotamer), 7.23 (s, 1H of both rotamers), 6.95 (s, 1H of both rotamers), 4.86-4.74 (m, 2H of both rotamers), 4.44 (s, 1H of minor rotamer), 4.06-3.98 (m, 1H of major rotamer), 3.58-3.51 (m, 1H of major rotamer), 3.43-3.34 (m, 1H of both rotamers and 1H minor rotamer), 2.01-1.83 (m, 2H of both rotamers), 1.79-1.66 (m, 1H of both rotamers), 1.64-1.57 (m, 1H of minor rotamer), 1.54-1.46 (m, 1H of major rotamer), 1.41 (s, 9H of both rotamers), 1.10 (d, J=6.2 Hz, 3H of major rotamer), 0.95 (d, J=6.4 Hz, 3H of minor rotamer).

Example 304 5-(4-(Difluoromethyl)-6-(((R)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62, Step A, substituting (R)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 138) and N—((S)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 139) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S 563.2 m/z, found 564.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆, 80° C.) δ 8.09 (s, 1H), 7.92-7.80 (m, 1H), 7.55 (d, J=9.0 Hz, 1H), 7.10-6.77 (m, 2H), 5.02 (d, J=15.3 Hz, 1H), 4.49 (s, 1H), 4.19-3.87 (m, 2H), 3.47-3.33 (m, 2H), 2.05-1.81 (m, 2H), 1.77-1.42 (m, 2H), 1.36 (d, J=7.0 Hz, 3H), 1.22-1.17 (m, 6H), 1.15 (s, 3H), 1.13-1.08 (m, 2H), 1.07-1.00 (m, 1H).

Example 305 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)-N-((5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)methyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 302, substituting 5-(aminomethyl)-1,3,4-oxadiazol-2(3H)-one hydrochloride for 5-(aminomethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one hydrochloride. MS (ESI): mass calcd. for C₂₃H₂₆F₃N₇₀₄S, 553.2; m/z found, 553.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃, mixture of rotamers) δ 10.17 (br s, 1H of major rotamer), 10.05 (s, 1H of minor rotamer), 8.15 (s, 1H of both rotamers), 8.00 (t, J=6.2 Hz, 1H of major rotamer), 7.82 (t, J=6.2 Hz, 1H of minor rotamer), 6.651 (s, 1H of minor rotamer), 6.645 (s, 1H of major rotamer), 4.99 (s, 1H of minor rotamer), 4.97 (s, 1H of major rotamer), 4.67-4.52 (m, 2H of both rotamers), 4.27-4.18 (m, 1H of major rotamer), 4.18-4.10 (m, 1H of minor rotamer), 3.61-3.55 (m, 2H both of minor rotamer), 3.37-3.29 (m, 1H of major rotamer), 3.27-3.18 (m, 1H of major rotamer), 2.10-1.43 (m, 4H of both rotamers), 1.46 (s, 9H of both rotamers), 1.22 (d, J=6.2 Hz, 3H of major rotamer), 1.03 (d, J=6.4 Hz, 3H of minor rotamer).

Example 306 5-(4-(Difluoromethyl)-6-(((R)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62, Step A, substituting (R)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 138) and N—((R)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 132) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₀F₅N₅O₃S 563.2, m/z found 564.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.10 (d, J=9.5 Hz, 1H), 8.05 (s, 1H), 7.75 (d, J=8.8 Hz, 1H), 7.13-6.81 (m, 2H), 5.06-4.94 (m, 1H), 4.71 (br. s, 1H), 4.24-3.82 (m, 2H), 2.07-1.49 (m, 4H), 1.46-1.36 (m, 1H), 1.30 (d, J=6.8 Hz, 3H), 1.17-1.06 (m, 10H), 1.04 (d, J=6.4 Hz, 2H), 0.93 (d, J=6.4 Hz, 1H).

Example 307 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-methyl-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 302, substituting aqueous methylamine (40% w/w, 5 equiv.) for 5-(aminomethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one hydrochloride and omitting DIPEA. MS (ESI): mass calcd. for C₂₁H₂₆F₃N₅O₂S, 469.2; m/z found, 469.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃, mixture of rotamers) δ 7.96 (s, 1H of major rotamer), 7.95 (s, 1H of minor rotamer), 7.14 (appar q, J=5.1 Hz, 1H of major rotamer), 7.13 (s, 1H of minor rotamer), 7.10 (s, 1H of major rotamer), 7.08-7.03 (m, 1H of minor rotamer), 6.02 (br s, NH), 4.68-4.61 (m, 1H of minor rotamer), 4.23-4.16 (m, 1H of major rotamer), 3.79-3.72 (m, 1H of major rotamer), 3.63-3.50 (m, 1H of both rotamers, 1H of minor rotamer), 3.10-3.04 (m, 3H of both rotamers), 2.12-2.04 (m, 1H of both rotamers), 2.03-1.77 (m, 2H of both rotamers), 1.75-1.68 (m, 1H of minor rotamer), 1.63-1.55 (m, 1H of major rotamer), 1.52 (s, 9H of both rotamers), 1.25 (d, J=6.2 Hz, 3H of major rotamer), 1.11 (d, J=6.4 Hz, 3H of minor rotamer).

Example 308 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 302, substituting aqueous ammonia (33% w/w, 5 equiv.) for 5-(aminomethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one hydrochloride and omitting DIPEA. MS (ESI): mass calcd. for C₂H₂₄F₃N₅O₂S, 455.2; m/z found, 456.0 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃, mixture of rotamers) δ 8.18 (s, 1H of both rotamers), 7.12 (s, 1H of major rotamer), 7.04 (s, 1H of minor rotamer), 6.64 (s, 1H of minor rotamer), 6.63 (s, 1H of major rotamer), 5.97 (s, 1H of minor rotamer), 5.93 (s, 1H of major rotamer), 4.95 (s, 1H of both rotamers), 4.34-4.27 (m, 1H of minor rotamer), 4.25-4.17 (m, 1H of major rotamer), 3.64-3.52 (m, 2H both of minor rotamers), 3.52-3.45 (m, 1H of major rotamer), 3.44-3.38 (m, 1H of major rotamer), 2.10-1.49 (m, 4H of both rotamers), 1.46 (s, 9H of both rotamers), 1.24 (d, J=6.3 Hz, 3H of major rotamer), 1.09 (d, J=6.4 Hz, 3H of minor rotamer).

Example 309 (S)-5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-ethyl-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 302, substituting ethylamine (5 equiv.) for 5-(aminomethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one hydrochloride and omitting DIPEA. MS (ESI): mass calcd. for C₂₂H₂₈F₃N₅O₂S, 483.2; m/z found, 484.0 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃, mixture of rotamers) δ 7.98 (s, 1H of major rotamer), 7.96 (s, 1H of minor rotamer), 7.14 (t, J=6.0 Hz, 1H of major rotamer), 7.10 (s, 1H of minor rotamer), 7.07 (s, 1H of major rotamer), 7.05 (t, J=5.9 Hz, 1H of minor rotamer), 5.92 (br s, NH), 4.62-4.55 (m, 1H of minor rotamer), 4.23-4.16 (m, 1H of major rotamer), 3.75-3.68 (m, 1H of major rotamer), 3.63-3.47 (m, 3H of both rotamers, 1H of minor rotamer), 2.12-2.03 (m, 1H of both rotamers), 2.03-1.77 (m, 2H of both rotamers), 1.74-1.68 (m, 1H of minor rotamer), 1.62-1.55 (m, 1H of major rotamer), 1.52 (s, 9H of minor rotamer), 1.52 (s, 9H of major rotamer), 1.31 (t, J=7.3 Hz, 3H of both rotamers), 1.26 (d, J=6.2 Hz, 3H of major rotamer), 1.13 (d, J=6.4 Hz, 3H of minor rotamer).

Example 310 5-(6-(((S)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-((1r,3S)-3-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149, substituting ethyl 5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 128) and trans-3-aminocyclobutanol HCl for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.2; m/z found, 574.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃, mixture of rotamers) δ 8.85 (br s, 1H of minor rotamer), 8.58 (br s, 1H of major rotamer), 7.91 (s, 1H of major rotamer), 7.87 (s, 1H of minor rotamer), 7.24 (d, J=7.1 Hz, 1H of major rotamer), 7.19 (d, J=7.0 Hz, 1H of minor rotamer), 7.03-6.72 (m, CHF₂ of both rotamers), 6.94 (s, 1H of minor rotamer), 6.92 (s, 1H of major rotamer), 4.72-4.64 (m, 1H of both rotamers), 4.64-4.58 (m, 1H of both rotamers), 4.52-4.45 (m, 1H of minor rotamer), 4.24-4.17 (m, 1H of major rotamer), 3.72-3.55 (m, 2H of both rotamers plus 1H of minor rotamer), 3.49-3.43 (m, 1H of major rotamer), 3.26 (br s, OH), 2.55-2.41 (m, 4H of both rotamers), 2.15-2.05 (m, 1H of both rotamers), 2.05-1.89 (m, 1H of both rotamers plus 1H of minor rotamer), 1.89-1.79 (m, 1H of major rotamer), 1.75-1.68 (m, 1H of minor rotamer), 1.64-1.55 (m, 1H of major rotamer), 1.39-1.28 (m, 1H of both rotamers), 1.25 (d, J=6.3 Hz, 3H of major rotamer), 1.04 (d, J=6.4 Hz, 3H of minor rotamer), 0.88-0.80 (m, 1H of both rotamers), 0.79-0.70 (m, 1H of both rotamers), 0.65-0.58 (m, 1H of both rotamers), 0.46-0.39 (m, 1H of both rotamers).

Example 311 5-(6-(((S)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl 5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 128) and (R)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃, mixture of rotamers) δ 9.45 (br s, 1H of minor rotamer), 9.16 (br s, 1H of major rotamer), 7.89 (s, 1H of major rotamer), 7.86 (s, 1H of minor rotamer), 7.43-7.36 (m, 1H of both rotamers), 7.00-6.72 (m, CHF₂ of both rotamers), 6.97 (s, 1H of minor rotamer), 6.96 (s, 1H of major rotamer), 4.80 (br s, OH), 4.65-4.57 (m, 1H of minor rotamer), 4.24-4.15 (m, 1H of major rotamer), 4.14-4.04 (m, 1H of both rotamers), 3.79-3.71 (m, 1H of major rotamer), 3.63-3.47 (m, 2H of both rotamers plus 1H of minor rotamer), 2.15-2.05 (m, 1H of both rotamers), 2.04-1.89 (m, 1H of both rotamers plus 1H of minor rotamer), 1.89-1.80 (m, 1H of major rotamer), 1.75-1.69 (m, 1H of minor rotamer), 1.64-1.56 (m, 1H of major rotamer), 1.41-1.33 (m, 1H of both rotamers), 1.33-1.29 (m, 9H of both rotamers), 1.26 (d, J=6.3 Hz, 3H of major rotamer), 1.11 (d, J=6.4 Hz, 3H of minor rotamer), 0.89-0.81 (m, 1H of both rotamers), 0.81-0.72 (m, 1H of both rotamers), 0.66-0.59 (m, 1H of both rotamers), 0.46-0.38 (m, 1H of both rotamers).

Example 312 5-(6-(((S)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl 5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 128) and (S)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S, 589.2; m/z found, 590.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃, mixture of rotamers) δ 10.05 (br s, 1H of minor rotamer), 9.86 (br s, 1H of major rotamer), 7.92 (s, 1H of major rotamer), 7.91 (s, 1H of minor rotamer), 7.40 (d, J=9.1 Hz, 1H of both rotamers), 7.03 (s, 1H of minor rotamer), 7.02 (s, 1H of major rotamer), 6.98-6.72 (m, CHF₂ of both rotamers), 6.94 (br s, OH), 4.65-4.57 (m, 1H of minor rotamer), 4.23-4.16 (m, 1H of major rotamer), 4.14-4.07 (m, 1H of both rotamers), 3.86-3.80 (m, 1H of major rotamer), 3.63-3.52 (m, 1H of both rotamer plus 1H of minor rotamer), 3.46-3.35 (m, 1H of both rotamers), 2.16-2.06 (m, 1H of both rotamers), 2.06-1.92 (m, 1H of both rotamers plus 1H of minor rotamer), 1.92-1.82 (m, 1H of major rotamer), 1.77-1.71 (m, 1H of minor rotamer), 1.66-1.59 (m, 1H of major rotamer), 1.43-1.36 (m, 1H of both rotamers), 1.35-1.29 (m, 9H of both rotamers), 1.27 (d, J=6.3 Hz, 3H of major rotamer), 1.13 (d, J=6.4 Hz, 3H of minor rotamer), 0.91-0.84 (m, 1H of both rotamers), 0.83-0.75 (m, 1H of both rotamers), 0.68-0.60 (m, 1H of both rotamers), 0.47-0.40 (m, 1H of both rotamers).

Example 313 5-(6-(((S)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl 5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 129) and (S)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₆H₃₀F₇N₅₃S, 625.2; m/z found, 626.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃, mixture of rotamers) δ 8.16 (br s, 1H of both rotamers), 7.92 (s, 1H of major rotamer), 7.90 (s, 1H of minor rotamer), 7.35 (d, J=9.2 Hz, 1H of both rotamers), 6.92-6.63 (m, CHF₂ of both rotamers), 6.90 (s, 1H of minor rotamer), 6.89 (s, 1H of major rotamer), 4.84-4.75 (m, 1H of minor rotamer), 4.54-4.46 (m, 1H of major rotamer), 4.22-4.05 (m, 2H of both rotamers), 4.05-3.95 (m, 1H of major rotamer), 3.88-3.78 (m, 1H of minor rotamer), 3.78-3.68 (m, 1H of both rotamers), 2.92 (br s, OH), 2.71-2.51 (m, 1H of both rotamers), 2.24-2.15 (m, 1H of minor rotamer), 2.11 (qd, J=13.9, 5.4 Hz, 1H of major rotamer), 1.38 (d, J=6.5 Hz, 3H of major rotamer), 1.35-1.24 (m, 10H of both rotamers plus 3H of minor rotamer), 0.86-0.79 (m, 1H of both rotamers), 0.77-0.69 (m, 1H of both rotamers), 0.65-0.57 (m, 1H of both rotamers), 0.46-0.38 (m, 1H of both rotamers).

Example 314 5-(6-(((S)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl 5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 129) and (R)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₆H₃₀F₇N₅₃S, 625.2; m/z found, 626.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃, mixture of rotamers) δ 8.95 (br s, 1H of both rotamers), 7.92 (s, 1H of major rotamer), 7.90 (s, 1H of minor rotamer), 7.43-7.36 (m, 1H of both rotamers), 6.95 (s, 1H of minor rotamer), 6.94 (s, 1H of major rotamer), 6.91-6.63 (m, CHF₂ of both rotamers), 4.96-4.88 (m, 1H of minor rotamer), 4.54-4.45 (m, 1H of major rotamer), 4.28-4.17 (m, 1H of major rotamer), 4.13-3.97 (m, 2H of both rotamers), 3.89-3.79 (m, 1H of minor rotamer), 3.59 (br s, 1H of both rotamers), 3.37 (br s, OH), 2.72-2.51 (m, 1H of both rotamers), 2.21 (td, J=16.1, 15.3, 6.9 Hz, 1H of minor rotamer), 2.11 (qd, J=13.8, 5.1 Hz, 1H of major rotamer), 1.38 (d, J=6.4 Hz, 13H of both rotamers), 0.89-0.81 (m, 1H of both rotamers), 0.80-0.73 (m, 1H of both rotamers), 0.66-0.59 (m, 1H of both rotamers), 0.46-0.39 (m, 1H of both rotamers).

Example 315 5-(6-(((S)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-((1r,3S)-3-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149, substituting ethyl 5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 129) and trans-3-aminocyclobutanol HCl for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₅H₂₆F₇N₅O₃S, 609.2; m/z found, 610.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃, mixture of rotamers) δ 9.05 (br s, 1H of both rotamers), 7.93 (s, 1H of major rotamer), 7.92 (s, 1H of minor rotamer), 7.20-7.13 (m, 1H of both rotamers), 6.96 (s, 1H of minor rotamer), 6.95 (s, 1H of major rotamer), 6.94-6.62 (m, CHF₂ of both rotamers), 4.86-4.41 (m, 4H of both rotamers), 4.27-4.16 (m, 1H of major rotamer), 4.10-3.92 (m, 1H of both rotamers), 3.90-3.80 (m, 1H of minor rotamer), 3.58 (br s, 1H of both rotamers), 2.80-2.54 (m, 1H of both rotamers), 2.54-2.41 (m, 4H of both rotamers), 2.26-2.06 (m, 1H of both rotamers), 1.38 (d, J=6.5 Hz, 3H of major rotamer), 1.38-1.31 (m, 1H of both rotamers), 1.23 (d, J=6.6 Hz, 3H of minor rotamer), 0.89-0.82 (m, 1H of both rotamers), 0.80-0.72 (m, 1H of both rotamers), 0.67-0.59 (m, 1H of both rotamers), 0.46-0.38 (m, 1H of both rotamers).

Example 316 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 130) and (R)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₇H₃₂F₅N₅O₃S, 601.2; m/z found, 602.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.56 (s, 1H), 7.91 (br s, 1H), 7.44 (d, J=9.1 Hz, 1H), 6.92 (s, 1H), 6.83 (t, J=54.7 Hz, 1H), 4.68 (t, J=4.1 Hz, 1H), 4.62 (t, J=4.0 Hz, 1H), 4.08 (dq, J=9.1, 6.7 Hz, 1H), 3.85 (br s, 1H), 3.72-3.61 (m, 1H), 1.88-1.70 (m, 4H), 1.59-1.46 (m, 4H), 1.36-1.28 (m, 10H), 0.87-0.79 (m, 1H), 0.77-0.70 (m, 1H), 0.65-0.58 (m, 1H), 0.45-0.38 (m, 1H).

Example 317 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148, substituting ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 130) and (S)-3-amino-2-methylbutan-2-ol for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and (R)-(−)-2-amino-1-propanol. MS (ESI): mass calcd. for C₂₇H₃₂F₅N₅O₃S, 601.2; m/z found, 602.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.65 (br s, 1H), 7.90 (s, 1H), 7.43 (d, J=9.1 Hz, 1H), 6.93 (s, 1H), 6.82 (t, J=54.7 Hz, 1H), 4.68 (t, J=4.1 Hz, 1H), 4.63 (t, J=4.3 Hz, 1H), 4.08 (dq, J=9.2, 6.8 Hz, 1H), 3.69-3.60 (m, 1H), 3.45 (br s, 1H), 1.88-1.72 (m, 4H), 1.58-1.47 (m, 4H), 1.37-1.27 (m, 10H), 0.87-0.80 (m, 1H), 0.78-0.70 (m, 1H), 0.65-0.58 (m, 1H), 0.45-0.39 (m, 1H).

Example 318 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-((1r,3S)-3-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149, substituting ethyl 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 130) and trans-3-aminocyclobutanol HCl for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₆H₂₈F₅N₅O₃S, 585.2; m/z found, 586.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 7.94 (s, 1H), 7.65 (br s, 1H), 7.25 (d, J=7.5 Hz, 1H), 6.88 (s, 1H), 6.80 (t, J=54.7 Hz, 1H), 4.71-4.64 (m, 2H), 4.64-4.58 (m, 1H), 4.46-4.40 (m, 1H), 3.89-3.78 (m, 1H), 3.06 (br s, 1H), 2.52-2.41 (m, 4H), 1.86-1.60 (m, 4H), 1.56-1.45 (m, 4H), 1.32-1.23 (m, 1H), 0.86-0.77 (m, 1H), 0.74-0.66 (m, 1H), 0.64-0.57 (m, 1H), 0.45-0.37 (m, 1H).

Example 319 5-(4-(Difluoromethyl)-6-(((R)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1r,3S)-3-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149, substituting ethyl 5-(4-(difluoromethyl)-6-(((R)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 149) and trans-3-aminocyclobutanol HCl for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S 547.2, m/z found 548.0 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.11-8.00 (m, 1H), 7.33 (d, J=7.3 Hz, 1H), 7.03-6.58 (m, 2H), 5.02-4.86 (m, 2H), 4.70-4.54 (m, 2H), 4.29-4.15 (m, 1H), 3.61-3.27 (m, 2H), 2.50-2.39 (m, 4H), 2.11-1.87 (m, 3H), 1.82-1.70 (m, 1H), 1.59-1.48 (m, 1H), 1.45-1.36 (m, 3H), 1.25-1.20 (m, 2H), 1.00 (d, J=6.2 Hz, 1H).

Example 320 5-(6-(((R)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-((1r,3S)-3-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepare as escribed in Example 149, substituting ethyl 5-(6-(((R)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 148) and trans-3-aminocyclobutanol HCl for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S 573.2, m/z found 574.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.06-7.98 (m, 1H), 7.37-7.28 (m, 1H), 7.06-6.62 (m, 2H), 5.01 (d, J=9.3 Hz, 1H), 4.73-4.54 (m, 2H), 4.41-4.15 (m, 2H), 3.62-3.28 (m, 2H), 2.55-2.36 (m, 4H), 2.19-1.70 (m, 4H), 1.59-1.48 (m, 1H), 1.32-1.19 (m, 2H), 1.18-1.06 (m, 1H), 1.00 (d, J=6.4 Hz, 1H), 0.82-0.69 (m, 1H), 0.64-0.51 (m, 2H), 0.47-0.34 (m, 1H).

Example 321 5-(4-(Difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62: Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and N—((R)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 132) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)-pyridin-2-amine and (S)-ethyl 4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₅F₂N₅O₃S 535.2, m/z found 536.0 [M+H]⁺. ¹H NMR (500 MHz, DMSO-d₆) δ 8.13-8.01 (m, 1H), 7.96 (s, 1H), 7.45 (s, 1H), 7.11-6.77 (m, 1H), 6.67 (s, 1H), 4.73-4.66 (m, 1H), 4.04-3.84 (m, 2H), 3.29-3.18 (m, 2H), 2.28-2.18 (m, 2H), 2.05-1.90 (m, 3H), 1.85-1.74 (m, 3H), 1.68-1.55 (m, 1H), 1.50-1.40 (m, 4H), 1.15-1.04 (m, 11H), 0.93 (d, J=6.4 Hz, 1H).

Example 322 5-(4-(Difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62: Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and N—((S)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 139) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)-pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₅F₂N₅O₃S 535.2, m/z found 536.0 [M+H]⁺. ¹H NMR (500 MHz, DMSO-d₆, 80° C.) δ 8.01 (s, 1H), 7.91-7.78 (m, 1H), 7.20 (s, 1H), 7.06-6.74 (m, 1H), 6.72 (s, 1H), 4.50 (br s, 1H), 4.16-4.01 (m, 1H), 3.98-3.85 (m, 1H), 3.52-3.26 (m, 2H), 2.36-2.27 (m, 2H), 2.07-1.67 (m, 7H), 1.55-1.45 (m, 4H), 1.23-1.17 (m, 6H), 1.16 (s, 3H), 1.14-1.09 (m, 2H), 1.06-0.99 (m, 1H).

Example 323 5-(4-(Difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N-((1r,3S)-3-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium (S)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 133), trans-3-aminocyclobutanol HCl, and THF for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid, 4-aminotetrahydro-2H-thiopyran-1,1-dioxide HCl, and DMF. MS (ESI): mass calcd. for C₂₅H₃₁F₂N₅O₃S 519.2 m/z, found 520.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.17-9.12 (m, 1H), 7.98 (s, 1H), 7.45 (s, 1H), 7.16-6.77 (m, 1H), 6.68 (s, 1H), 5.07-5.00 (m, 1H), 4.54-4.41 (m, 1H), 4.36-4.14 (m, 1H), 4.06-3.96 (m, 1H), 3.30-3.24 (m, 2H), 2.44-2.35 (m, 2H), 2.29-2.19 (m, 2H), 2.18-2.09 (m, 2H), 2.07-1.90 (m, 3H), 1.88-1.76 (m, 3H), 1.73-1.56 (m, 1H), 1.54-1.41 (m, 4H), 1.08 (d, J=6.2 Hz, 2H), 0.86 (d, J=6.4 Hz, 1H).

Example 324 (S)-5-(4-(Difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62: Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and (S)—N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 134) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₄S₂, 581.2, m/z found 582.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.04 (d, J=8.4 Hz, 1H), 7.96 (s, 1H), 7.45 (s, 1H), 7.13-6.75 (m, 1H), 6.67 (s, 1H), 4.26-4.13 (m, 2H), 4.04-3.95 (m, 1H), 3.31 (s, 3H), 3.11-3.02 (m, 2H), 2.29-2.13 (m, 4H), 2.12-1.90 (m, 5H), 1.87-1.74 (m, 3H), 1.69-1.59 (m, 1H), 1.54-1.37 (m, 4H), 1.06 (d, J=6.4 Hz, 2H), 0.85 (d, J=6.4 Hz, 1H).

Example 325 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62: Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide (Intermediate 135) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₃F₄N₅O₃S 571.2 m/z, found 572.0 [M+H]⁺. ¹H NMR (500 MHz, DMSO-d₆) δ 8.16-8.02 (m, 1H), 7.98 (s, 1H), 7.47 (s, 1H), 7.07-6.74 (m, 1H), 6.70 (s, 1H), 4.80-4.71 (m, 1H), 4.61-4.24 (m, 1H), 4.02-3.80 (m, 3H), 2.65-2.53 (m, 2H), 2.30-2.21 (m, 2H), 2.09-1.97 (m, 2H), 1.91-1.75 (m, 2H), 1.49 (s, 3H), 1.24-1.20 (m, 3H), 1.18-1.11 (m, 9H)

Example 326 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62: Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide (Intermediate 140) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₃F₄N₅O₃S 571.2, m/z found 572.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.10-8.01 (m, 1H), 8.01-7.95 (m, 1H), 7.47 (s, 1H), 7.07-6.76 (m, 1H), 6.69 (s, 1H), 4.76-4.68 (m, 1H), 4.50-4.25 (m, 1H), 4.03-3.76 (m, 3H), 2.65-2.54 (m, 2H), 2.31-2.20 (m, 2H), 2.08-1.97 (m, 2H), 1.88-1.77 (m, 2H), 1.49 (s, 3H), 1.22 (d, J=6.4 Hz, 3H), 1.18-1.08 (m, 9H).

Example 327 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N-((1r,3S)-3-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149, substituting ethyl (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 136) and trans-3-aminocyclobutanol HCl for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate and 3-hydroxy-3-methylazetidine HCl. MS (ESI): mass calcd. for C₂₅H₂₉F₄N₅O₃S 555.2 m/z, found 556.0 [M+H]⁺. ¹H NMR (500 MHz, DMSO-d₆) δ 9.16-9.03 (m, 1H), 7.94 (s, 1H), 7.49-7.38 (m, 1H), 7.05-6.70 (m, 1H), 6.65 (s, 1H), 5.02 (d, J=5.1 Hz, 1H), 4.62-4.38 (m, 1H), 4.34-4.22 (m, 2H), 4.11-3.98 (m, 1H), 3.94-3.78 (m, 1H), 2.61-2.52 (m, 2H), 2.41-2.33 (m, 2H), 2.27-2.17 (m, 2H), 2.14-2.06 (m, 2H), 2.03-1.93 (m, 2H), 1.86-1.73 (m, 2H), 1.46 (s, 3H), 1.22-0.97 (m, 3H).

Example 328 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)thiazole-2-carboxamide

The title compound was prepare as described in Intermediate 62: Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)thiazole-2-carboxamide (Intermediate 142) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₁F₄N₅O₄S₂ 617.2 m/z, found 618.0 [M+H]⁺. ¹H NMR (500 MHz, DMSO-d₆, 80° C.) δ 8.82-8.65 (m, 1H), 8.00 (s, 1H), 7.20 (s, 1H), 7.04-6.66 (m, 2H), 4.67-3.82 (m, 4H), 3.39-3.24 (m, 2H), 3.19-3.13 (m, 2H), 2.69-2.53 (m, 2H), 2.38-2.23 (m, 4H), 2.20-2.13 (m, 2H), 2.10-2.01 (m, 2H), 1.94-1.78 (m, 2H), 1.52 (s, 3H), 1.33-1.07 (m, 3H).

Example 329 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62: Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide (Intermediate 143) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₇H₃₅F₂N₅O₃S 547.2, m/z found 548.0 [M+H]⁺. ¹H NMR (500 MHz, DMSO-d₆) δ 8.07 (d, J=9.5 Hz, 1H), 7.98 (s, 1H), 7.49 (s, 1H), 7.13-6.69 (m, 2H), 4.74 (s, 1H), 4.48 (br s 1H), 4.05 (br s 1H), 3.96-3.86 (m, 1H), 2.31-2.19 (m, 2H), 2.08-1.98 (m, 2H), 1.89-1.75 (m, 2H), 1.49 (s, 5H), 1.44-1.22 (m, 6H), 1.20-1.09 (m, 9H).

Example 330 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N-((1r,3R)-3-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 145), trans-3-aminocyclobutanol HCl, and THF for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid, 4-aminotetrahydro-2H-thiopyran-1,1-dioxide HCl, and DMF. MS (ESI): mass calcd. for C₂₆H₃₁F₂N₅O₃S 531.2 m/z, found 532.0 [M+H]⁺. ¹H NMR (500 MHz, DMSO-d₆) δ 9.14 (d, J=7.3 Hz, 1H), 7.94 (s, 1H), 7.46 (s, 1H), 7.11-6.79 (m, 1H), 6.68 (s, 1H), 5.00 (d, J=5.3 Hz, 1H), 4.50-4.38 (m, 2H), 4.32-4.21 (m, 1H), 3.97-3.87 (m, 1H), 2.40-2.32 (m, 2H), 2.26-2.15 (m, 2H), 2.14-2.06 (m, 2H), 2.04-1.95 (m, 2H), 1.84-1.74 (m, 2H), 1.48-1.24 (m, 9H), 1.22-1.08 (m, 2H).

Example 331 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-((1-methylcyclobutyl)amino)pyridin-3-yl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62: Step A, substituting 5-bromo-4-(difluoromethyl)-N-(1-methylcyclobutyl)pyridin-2-amine (Intermediate 131) and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)thiazole-2-carboxamide (Intermediate 147) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₇H₃₃F₂N₅O₄S₂, 593.2, m/z found 594.2 [M+H]⁺. ¹H NMR (500 MHz, DMSO-d₆) δ 9.05 (d, J=8.6 Hz, 1H), 7.95 (s, 1H), 7.46 (s, 1H), 7.09-6.82 (m, 1H), 6.70 (s, 1H), 4.46-4.44 (m, 1H), 4.25-4.13 (m, 1H), 3.98-3.96 (m, 1H), 3.37-3.31 (m, 2H), 3.11-3.02 (m, 2H), 2.29-2.15 (m, 4H), 2.10-1.95 (m, 4H), 1.86-1.75 (m, 2H), 1.48-1.26 (m, 9H), 1.24-1.12 (m, 2H).

Example 332 5-(6-(((R)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N—((R)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62: Step A, substituting (R)-5-bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 137) and N—((R)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 132) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S 589.2, m/z found 590.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.17-8.06 (m, 1H), 8.03 (s, 1H), 7.92-7.81 (m, 1H), 7.19-6.76 (m, 2H), 4.75-4.67 (m, 1H), 4.56-4.42 (m, 1H), 4.26-3.87 (m, 2H), 3.45-3.36 (m, 1H), 3.32-3.23 (m, 1H), 2.01-1.54 (m, 3H), 1.50-1.38 (m, 1H), 1.20-1.09 (m, 10H), 1.06 (d, J=6.4 Hz, 2H), 0.95 (d, J=6.4 Hz, 1H), 0.70-0.60 (m, 1H), 0.58-0.46 (m, 2H), 0.39-0.27 (m, 1H).

Example 333 5-(6-(((R)-1-Cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N—((S)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 62: Step A, substituting (R)-5-bromo-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(difluoromethyl)pyridin-2-amine (Intermediate 137) and N—((S)-3-hydroxy-3-methylbutan-2-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 139) for 5-bromo-N-cyclopentyl-4-(difluoromethyl)pyridin-2-amine and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₂F₅N₅O₃S 589.2, m/z found 590.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆, 80° C.) δ 8.06 (s, 1H), 7.94-7.81 (m, 1H), 7.62 (d, J=8.5 Hz, 1H), 7.11-6.77 (m, 2H), 4.61-4.46 (m, 2H), 4.18-3.88 (m, 2H), 3.47-3.30 (m, 2H), 2.04-1.81 (m, 2H), 1.77-1.40 (m, 2H), 1.22-1.15 (m, 10H), 1.13-1.01 (m, 3H), 0.71-0.62 (m, 1H), 0.59-0.45 (m, 2H), 0.44-0.35 (m, 1H).

Example 334 5-[6-(2,2-Dimethylpropylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-4-(2-methylpyrrolidine-1-carbonyl)-5-(6-(neopentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 150) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₆F₃N₅O₃S, 555.7; m/z found, 556.3 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.13 (s, 1H), 7.45 (d, J=9.3 Hz, 1H), 6.68-6.62 (m, 1H), 4.39-4.15 (m, 1H), 4.14-4.03 (m, 1H), 3.65-3.38 (m, 2H), 3.27-3.05 (m, 2H), 2.42-2.26 (m, 1H), 2.12-2.01 (m, 1H), 1.97-1.84 (m, 1H), 1.81-1.69 (m, 1H), 1.60-1.48 (m, 1H), 1.34-1.22 (m, 12H), 1.12 (d, J=6.4 Hz, 1H), 1.01-0.94 (m, 9H).

Example 335 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₃S, 541.6; m/z found, 542.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19-8.14 (m, 1H), 7.44 (d, J=9.2 Hz, 1H), 6.66-6.62 (m, 1H), 4.32-4.03 (m, 2H), 3.66-3.33 (m, 2H), 2.32-2.19 (m, 1H), 2.11-2.01 (m, 1H), 1.94-1.83 (m, 1H), 1.78-1.68 (m, 1H), 1.60-1.48 (m, 1H), 1.45 (s, 9H), 1.33-1.21 (m, 12H), 1.12 (d, J=6.3 Hz, 1H).

Example 336 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(1S)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (S)-3-amino-2-methylbutan-2-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₃S, 541.6; m/z found, 542.3 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.18-8.14 (s, 1H), 7.49-7.41 (dd, J=9.3, 3.5 Hz, 1H), 6.69-6.63 (s, 1H), 5.19-5.04 (m, 1H), 4.27-4.16 (m, 1H), 4.15-4.05 (m, 1H), 3.41-3.36 (m, 1H), 2.55-2.38 (m, 1H), 2.13-1.99 (m, 1H), 1.96-1.82 (m, 1H), 1.80-1.69 (m, 1H), 1.59-1.48 (m, 1H), 1.46-1.42 (s, 9H), 1.32-1.12 (m, 13H).

Example 337 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-(3-hydroxy-3-methyl-cyclobutyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (s,3s)-3-amino-1-methylcyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.3 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.16 (s, 1H), 7.54 (d, J=8.0 Hz, 1H), 6.66-6.64 (m, 1H), 5.09 (s, 1H), 4.23-4.16 (m, 2H), 3.41-3.35 (m, 1H), 2.92 (br s, 1H), 2.63-2.58 (m, 2H), 2.27-2.20 (m, 2H), 2.09-2.02 (m, 1H), 1.93-1.86 (m, 1H), 1.76-1.70 (m, 1H), 1.58-1.49 (m, 1H), 1.45-1.42 (m, 11H), 1.26-1.22 (m, 2H).

Example 338 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-(3-hydroxy-3-methyl-butyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 4-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₃S, 541.6; m/z found, 542.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.15 (s, 1H), 7.97-7.87 (m, 1H), 6.65 (s, 1H), 5.21-5.10 (m, 1H), 4.38-4.07 (m, 1H), 3.68-3.55 (m, 2H), 3.49-3.38 (m, 1H), 2.43-2.29 (m, 1H), 2.09-1.99 (m, 1H), 1.95-1.69 (m, 4H), 1.65-1.48 (m, 1H), 1.44 (s, 9H), 1.32-1.05 (m, 10H).

Example 339 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-(2-hydroxy-1,1-dimethyl-ethyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 2-amino-2-methylpropan-1-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₂F₃N₅O₃S, 527.6; m/z found, 528.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.18-8.13 (m, 1H), 7.36-7.29 (m, 1H), 6.68-6.62 (m, 1H), 5.12-5.04 (m, 1H), 4.27-4.08 (m, 2H), 3.72 (d, J=5.7 Hz, 2H), 3.36 (t, J=6.8 Hz, 1H), 2.10-2.02 (m, 1H), 1.97-1.82 (m, 1H), 1.80-1.67 (m, 1H), 1.56-1.42 (m, 16H), 1.30-1.09 (m, 4H).

Example 340 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-(2-hydroxy-2-methyl-propyl)-N-methyl-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 2-methyl-1-(methylamino)propan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₃S, 541.6; m/z found, 542.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19-8.13 (m, 1H), 6.69-6.58 (m, 1H), 5.15-5.01 (m, 1H), 4.27-3.89 (m, 2H), 3.75-3.43 (m, 5H), 3.28 (s, 1H), 2.14-1.49 (m, 5H), 1.44 (s, 9H), 1.34-1.22 (m, 9H).

Example 341 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(1R)-1,2-dimethylpropyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-methylbutan-2-amine for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₄F₃N₅O₂S, 525.6; m/z found, 526.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17 (s, 1H), 7.12-7.00 (m, 1H), 6.64 (s, 1H), 5.11-5.02 (m, 1H), 4.28-3.97 (m, 2H), 3.38 (t, J=6.7 Hz, 1H), 2.12-1.67 (m, 5H), 1.55-1.43 (m, 10H), 1.29-1.19 (m, 6H), 1.03-0.94 (m, 6H).

Example 342 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-(2-hydroxy-1,1,2-trimethyl-propyl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-amino-2,3-dimethylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₆F₃N₅O₃S, 555.7; m/z found, 556.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17 (d, J=3.4 Hz, 1H), 7.54-7.43 (m, 1H), 6.63 (s, 1H), 5.00-4.63 (m, 2H), 4.34-4.14 (m, 1H), 3.42-3.33 (m, 1H), 2.12-2.02 (m, 1H), 1.93-1.83 (m, 1H), 1.78-1.67 (m, 2H), 1.51-1.43 (m, 16H), 1.29-1.21 (m, 9H).

Example 343 5-[4-(Difluoromethyl)-6-(2,2-dimethylpropylamino)-3-pyridyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(4-(difluoromethyl)-6-(neopentylamino)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 151) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₇F₂N₅O₃S, 537.7; m/z found, 538.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.06-7.94 (m, 1H), 7.51-7.40 (m, 1H), 7.03-6.58 (m, 2H), 5.27-5.09 (m, 1H), 4.34-4.00 (m, 2H), 3.64-3.30 (m, 2H), 3.24-3.09 (m, 2H), 2.73-2.45 (m, 1H), 2.38-1.47 (m, 4H), 1.31-1.20 (m, 12H), 1.01-0.96 (m, 9H).

Example 344 5-[4-(Difluoromethyl)-6-(2,2-dimethylpropylamino)-3-pyridyl]-N-[(1S)-2-hydroxy-1,2-dimethyl-propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-3-amino-2-methylbutan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(4-(difluoromethyl)-6-(neopentylamino)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 151) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₇F₂N₅O₃S, 537.7; m/z found, 538.3 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.05-7.97 (m, 1H), 7.51-7.43 (m, 1H), 7.01-6.60 (m, 2H), 5.32-5.20 (m, 1H), 4.24-4.05 (m, 2H), 3.63-3.31 (m, 2H), 3.25-3.11 (m, 2H), 2.76 (s, 1H), 2.10-1.47 (m, 4H), 1.36-1.18 (m, 12H), 1.03-0.95 (m, 9H).

Example 345 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(2R)-2,3-dihydroxypropyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-3-aminopropane-1,2-diol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₃F₃N₅O₄S, 529.6; m/z found, 530.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.07 (s, 1H), 7.87-7.72 (m, 1H), 6.62-6.55 (m, 1H), 5.07-4.97 (m, 1H), 4.19-3.99 (m, 1H), 3.90-3.72 (m, 2H), 3.63-3.41 (m, 5H), 3.29 (t, J=6.5 Hz, 1H), 2.03-1.90 (m, 1H), 1.86-1.72 (m, 1H), 1.70-1.59 (m, 1H), 1.49-1.32 (m, 10H), 1.22-0.94 (m, 4H).

Example 346 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(1R)-2-hydroxy-1-methyl-ethyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₃F₃N₅O₃S, 513.6; m/z found, 514.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20-8.12 (m, 1H), 7.47 (d, J=8.0 Hz, 1H), 6.66 (d, J=2.1 Hz, 1H), 5.21-5.10 (m, 1H), 4.31-4.07 (m, 2H), 3.81-3.60 (m, 2H), 3.41-3.27 (m, 2H), 2.11-1.99 (m, 1H), 1.96-1.80 (m, 1H), 1.79-1.67 (m, 1H), 1.58-1.41 (m, 10H), 1.37-1.07 (m, 7H).

Example 347 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[cis-2-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-4-aminotetrahydrofuran-3-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20-8.10 (m, 1H), 7.79-7.65 (m, 1H), 6.66 (s, 1H), 5.19-5.06 (m, 1H), 4.30-4.11 (m, 3H), 3.63-3.33 (m, 2H), 2.21-2.00 (m, 2H), 1.98-1.83 (m, 3H), 1.83-1.67 (m, 3H), 1.67-1.58 (m, 1H), 1.57-1.40 (m, 10H), 1.32-1.05 (m, 4H).

Example 348 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(3S,4R)-4-hydroxytetrahydrofuran-3-yl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3R,4S)-4-aminotetrahydrofuran-3-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₄S, 541.6; m/z found, 542.2 [M+H]⁺. ¹H NMR (400 MHz, CD30D) δ 8.13-8.06 (m, 1H), 7.91 (s, 1H), 6.85 (s, 1H), 4.48-4.33 (m, 2H), 4.23-4.02 (m, 3H), 3.89-3.80 (m, 1H), 3.76-3.68 (m, 1H), 3.64-3.26 (m, 2H), 2.18-1.85 (m, 3H), 1.83-1.72 (m, 1H), 1.65-1.54 (m, 2H), 1.47 (s, 9H), 1.40-1.02 (m, 3H).

Example 349 [5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-2-[(3R)-3-hydroxypyrrolidine-1-carbonyl]thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 148 substituting (R)-pyrrolidin-3-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₀F₃N₅O₃S, 525.6; m/z found, 526.2 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.11-8.03 (m, 1H), 6.60-6.52 (m, 1H), 5.02-4.93 (m, 1H), 4.56-4.39 (m, 1H), 4.36-4.21 (m, 1H), 4.19-4.00 (m, 3H), 3.81-3.64 (m, 2H), 3.53-3.37 (m, 2H), 3.19-2.99 (s, 1H), 2.06-1.90 (m, 3H), 1.88-1.78 (m, 1H), 1.51-1.42 (m, 1H), 1.41-1.34 (s, 9H), 1.23-1.11 (m, 3H).

Example 350 [5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-2-[(3S)-3-hydroxypyrrolidine-1-carbonyl]thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 148 substituting (S)-pyrrolidin-3-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₀F₃N₅O₃S, 525.6; m/z found, 526.2 [M+H]⁺. ¹HNMR (400 MHz, CDCl₃) δ 8.19-8.11 (m, 1H), 6.70-6.61 (m, 1H), 5.18-5.06 (s, 1H), 4.63-4.47 (m, 1H), 4.48-4.36 (m, 1H), 4.32-4.05 (m, 3H), 3.91-3.79 (m, 1H), 3.79-3.69 (m, 1H), 3.67-3.44 (m, 2H), 3.44-3.33 (m, 1H), 2.18-1.97 (m, 3H), 1.97-1.84 (m, 1H), 1.70-1.50 (m, 1H), 1.50-1.41 (s, 9H), 1.31-1.19 (m, 3H).

Example 351 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(1R,2R)-2-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,2R)-2-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.23-8.15 (s, 1H), 7.40-7.33 (m, 1H), 6.70-6.64 (m, 1H), 5.14-5.01 (s, 1H), 4.30-4.00 (m, 4H), 3.41-3.34 (t, J=6.8 Hz, 1H), 2.37-2.22 (m, 1H), 2.16-2.02 (m, 2H), 1.97-1.85 (m, 2H), 1.82-1.70 (m, 3H), 1.70-1.61 (m, 1H), 1.59-1.42 (s, 10H), 1.29-1.06 (m, 4H).

Example 352 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-4-(2-methylpyrrolidine-1-carbonyl)-N-(3,3,3-trifluoro-2-hydroxy-propyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-amino-1,1,1-trifluoropropan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₇F₆N₅O₃S, 567.6; m/z found, 568.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.23-8.17 (m, 1H), 7.75-7.60 (m, 1H), 6.72-6.64 (m, 1H), 5.00-4.90 (m, 1H), 4.29-4.20 (m, 2H), 4.20-4.12 (q, J=7.1 Hz, 1H), 4.05-3.95 (m, 1H), 3.68-3.57 (m, 1H), 3.47-3.36 (m, 1H), 2.12-2.07 (m, 1H), 2.01-1.87 (m, 1H), 1.84-1.73 (m, 1H), 1.67-1.60 (m, 2H), 1.54-1.47 (s, 9H), 1.34-1.07 (m, 3H).

Example 353 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-N—((S*)-3,3,3-trifluoro-2-hydroxypropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-amino-1,1,1-trifluoropropan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Chiralpak AD-H 5 μm 250×30 mm, Mobile phase: 90% CO₂, 10% i-PrOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₃H₂₇F₆N₅O₃S, 567.6; m/z found, 568.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.05-7.99 (m, 1H), 7.76-7.62 (m, 1H), 6.62-6.54 (s, 1H), 5.08-4.97 (s, 1H), 4.14-3.82 (m, 3H), 3.51-3.20 (m, 3H), 2.02-1.90 (m, 1H), 1.88-1.75 (m, 1H), 1.71-1.59 (m, 1H), 1.49-1.31 (m, 10H), 1.18-0.91 (m, 4H).

Example 354 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-N—((R*)-3,3,3-trifluoro-2-hydroxypropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 3-amino-1,1,1-trifluoropropan-2-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Chiralpak AD-H 5 μm 250×30 mm, Mobile phase: 90% CO₂, 10% i-PrOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₃H₂₇F₆N₅O₃S, 567.6; m/z found, 568.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.06-8.02 (m, 1H), 7.76-7.63 (m, 1H), 6.60-6.55 (m, 1H), 5.03-4.91 (m, 1H), 4.16-4.01 (m, 2H), 3.99-3.83 (m, 1H), 3.52-3.41 (m, 2H), 3.34-3.21 (m, 1H), 2.02-1.91 (m, 1H), 1.84-1.72 (m, 1H), 1.70-1.61 (m, 1H), 1.48-1.32 (m, 10H), 1.14-0.99 (m, 4H).

Example 355 N-(2-Amino-2-methyl-propyl)-5-[6-(tert-butylamino)-4-(trifluoromethyl)-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 2-methylpropane-1,2-diamine for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₃F₃N₆O₂S, 526.6; m/z found, 527.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.22-8.15 (s, 1H), 7.72-7.62 (m, 1H), 6.69-6.62 (s, 1H), 5.12-5.01 (m, 1H), 4.37-4.08 (m, 1H), 3.67-3.27 (m, 4H), 2.13-2.01 (m, 1H), 2.00-1.85 (m, 1H), 1.83-1.69 (m, 1H), 1.60-1.40 (m, 11H), 1.30-1.10 (m, 10H).

Example 356 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-(1-methylazetidin-3-yl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 1-methylazetidin-3-amine for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₁F₃N₆O₂S, 524.6; m/z found, 525.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.14-8.07 (m, 1H), 7.54-7.39 (m, 1H), 6.58-6.52 (m, 1H), 4.91-4.80 (m, 1H), 4.69-4.54 (m, 1H), 4.21-4.07 (m, 1H), 3.70-3.57 (m, 2H), 3.43-3.24 (m, 2H), 3.09-2.95 (m, 1H), 2.34-2.25 (m, 3H), 2.06-1.93 (m, 1H), 1.90-1.77 (m, 2H), 1.70-1.63 (m, 1H), 1.53-1.32 (m, 10H), 1.19-0.97 (m, 3H).

Example 357 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-N-(3,3,3-trifluoro-2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting 3-amino-1,1,1-trifluoro-2-methylpropan-2-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₉F₆N₅O₃S, 581.6; m/z found, 582.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.21-8.16 (s, 1H), 7.67-7.54 (m, 1H), 6.67-6.63 (d, J=2.5 Hz, 1H), 4.94-4.88 (s, 1H), 4.28-4.18 (m, 1H), 4.18-4.09 (q, J=7.2 Hz, 1H), 3.87-3.69 (m, 2H), 1.63-1.58 (m, 2H), 3.47-3.37 (m, 1H), 2.12-2.03 (m, 2H), 1.97-1.85 (m, 1H), 1.82-1.72 (m, 1H), 1.50-1.46 (s, 9H), 1.46-1.44 (s, 3H), 1.28-1.23 (m, 2H).

Example 358 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-N—((S*)-3,3,3-trifluoro-2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting 3-amino-1,1,1-trifluoro-2-methylpropan-2-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: CHIRALCEL OJ-H 5 μm 250×20 mm, Mobile phase: 90% CO₂, 10% mixture of ACN/MeOH 90/10 v/v). MS (ESI): mass calcd. for C₂₄H₂₉F₆N₅O₃S, 581.6; m/z found, 581.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.18-8.11 (m, 1H), 7.76-7.66 (m, 1H), 6.69-6.61 (s, 1H), 5.09-4.99 (m, 1H), 4.60-4.27 (s, 1H), 4.25-4.10 (m, 1H), 3.85-3.62 (m, 2H), 3.62-3.30 (m, 2H), 2.13-1.99 (m, 1H), 1.97-1.80 (m, 2H), 1.79-1.67 (m, 1H), 1.64-1.36 (m, 12H), 1.31-1.04 (m, 3H).

Example 359 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)-N—((R*)-3,3,3-trifluoro-2-hydroxy-2-methylpropyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting 3-amino-1,1,1-trifluoro-2-methylpropan-2-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: CHIRALCEL OJ-H 5 μm 250×20 mm, Mobile phase: 90% CO₂, 10% mixture of ACN/MeOH 90/10 v/v). MS (ESI): mass calcd. for C₂₄H₂₉F₆N₅O₃S, 581.6; m/z found, 581.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.18-8.08 (m, 1H), 7.83-7.66 (m, 1H), 6.70-6.59 (s, 1H), 5.11-5.01 (s, 1H), 4.78-4.48 (s, 1H), 4.31-4.10 (m, 1H), 3.86-3.72 (m, 1H), 3.72-3.59 (m, 1H), 3.60-3.28 (m, 2H), 2.12-1.98 (m, 1H), 1.98-1.80 (m, 1H), 1.80-1.66 (m, 1H), 1.66-1.35 (s, 13H), 1.25-1.04 (m, 3H).

Example 360 [5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-2-[(1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptane-5-carbonyl]thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 149 substituting (1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptane HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃F₃N₅O₃S, 537.6; m/z found, 538.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.17-8.13 (s, 1H), 6.65-6.59 (m, 1H), 5.00-4.93 (d, J=7.0 Hz, 1H), 4.76-4.70 (m, 1H), 4.24-4.08 (m, 2H), 4.05-3.88 (m, 3H), 3.72-3.62 (m, 1H), 3.51-3.42 (m, 2H), 2.12-1.86 (m, 5H), 1.82-1.71 (m, 1H), 1.48-1.42 (s, 9H), 1.29-1.20 (m, 3H).

Example 361 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(1S,3S)-3-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1S,3S)-3-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19-8.15 (s, 1H), 7.21-7.09 (m, 1H), 6.67-6.61 (m, 1H), 5.03-4.95 (s, 1H), 4.70-4.57 (m, 1H), 4.53-4.44 (s, 1H), 4.25-4.08 (m, 1H), 3.64-3.50 (m, 1H), 3.38-3.31 (t, J=6.7 Hz, 1H), 2.43-2.29 (m, 1H), 2.25-2.00 (m, 3H), 1.99-1.92 (s, 1H), 1.92-1.79 (m, 2H), 1.77-1.66 (m, 2H), 1.66-1.56 (m, 1H), 1.55-1.48 (m, 1H), 1.48-1.42 (s, 9H), 1.28-1.20 (m, 3H).

Example 362 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(1S)-2-hydroxy-1-methyl-ethyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-2-aminopropan-1-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₃F₃N₅O₃S, 513.6; m/z found, 514.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.12-8.05 (s, 1H), 7.40-7.27 (m, 1H), 6.61-6.54 (m, 1H), 5.04-4.92 (m, 1H), 4.19-4.01 (m, 2H), 3.70-3.45 (m, 2H), 3.33-3.25 (dd, J=7.3, 5.2 Hz, 1H), 3.03-2.86 (m, 1H), 2.04-1.90 (m, 2H), 1.87-1.72 (m, 1H), 1.70-1.59 (m, 1H), 1.48-1.33 (s, 10H), 1.28-0.94 (m, 6H).

Example 363 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(2S)-2,3-dihydroxypropyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-3-aminopropane-1,2-diol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₃F₃N₅O₄S, 529.6; m/z found, 530.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.18-8.12 (m, 1H), 7.94-7.81 (m, 1H), 6.69-6.61 (m, 1H), 5.18-5.10 (m, 1H), 4.30-4.08 (m, 1H), 3.95-3.86 (m, 2H), 3.69-3.58 (m, 4H), 3.55-3.49 (m, 1H), 3.41-3.33 (m, 1H), 2.08-2.00 (m, 1H), 1.94-1.81 (m, 1H), 1.76-1.68 (m, 1H), 1.54-1.40 (m, 10H), 1.27-1.02 (m, 4H).

Example 364 (5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-2-(3-hydroxy-3-methylpyrrolidine-1-carbonyl)thiazol-4-yl)((S)-2-methylpyrrolidin-1-yl)methanone

The title compound was prepared as described in Example 148 substituting 3-methylpyrrolidin-3-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.21-8.15 (m, 1H), 6.67-6.60 (m, 1H), 4.90-4.86 (s, 1H), 4.50-4.36 (m, 1H), 4.34-4.10 (m, 2H), 3.98-3.79 (m, 2H), 3.64-3.46 (m, 2H), 2.15-2.01 (m, 2H), 1.97-1.89 (m, 1H), 1.84-1.76 (m, 1H), 1.66-1.61 (s, 2H), 1.61-1.50 (m, 4H), 1.49-1.45 (s, 9H), 1.30-1.02 (m, 3H).

Example 365 (5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-2-((S*)-3-hydroxy-3-methylpyrrolidine-1-carbonyl)thiazol-4-yl)((S)-2-methylpyrrolidin-1-yl)methanone

The title compound was prepared as described in Example 148 substituting 3-methylpyrrolidin-3-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux Cellulose-2, 5 μm, 250×30 mm, Mobile phase: 50% CO₂, 50% mixture of ACN/MeOH 90/10 v/v). MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 539.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.19-8.11 (dd, J=3.2, 2.2 Hz, 1H), 6.68-6.58 (m, 1H), 5.10-4.98 (s, 1H), 4.58-4.24 (m, 1H), 4.25-4.11 (m, 1H), 3.92-3.75 (m, 2H), 3.62-3.43 (m, 2H), 2.81-2.55 (s, 1H), 2.17-1.81 (m, 5H), 1.79-1.55 (m, 1H), 1.52-1.38 (m, 13H), 1.26-1.01 (m, 3H).

Example 366 (5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-2-((R*)-3-hydroxy-3-methylpyrrolidine-1-carbonyl)thiazol-4-yl)-((S)-2-methylpyrrolidin-1-yl)methanone

The title compound was prepared as described in Example 148 substituting 3-methylpyrrolidin-3-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux Cellulose-2, 5 μm, 250×30 mm, Mobile phase: 50% CO₂, 50% mixture of ACN/MeOH 90/10 v/v). MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 539.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ8.20-8.10 (t, J=3.3 Hz, 1H), 6.67-6.59 (d, J=2.9 Hz, 1H), 5.11-5.00 (d, J=3.0 Hz, 1H), 4.43-4.29 (m, 1H), 4.29-4.13 (m, 2H), 3.94-3.76 (m, 2H), 3.60-3.45 (m, 2H), 2.15-1.68 (m, 6H), 1.58-1.41 (m, 13H), 1.26-1.06 (m, 3H).

Example 367 5-[6-(tert-Buylamino)-4-(trifluoromethyl)-3-pyridyl]-N-[(1S,3R)-3-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,3S)-3-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 540.2 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.20-8.13 (m, 1H), 7.94-7.86 (m, 1H), 6.69-6.64 (m, 1H), 5.16-5.06 (m, 1H), 4.61-4.48 (m, 1H), 4.48-4.40 (s, 1H), 4.24-4.09 (m, 1H), 3.66-3.37 (m, 2H), 2.92-2.73 (m, 1H), 2.23-2.09 (m, 2H), 2.07-2.03 (s, 1H), 1.98-1.71 (m, 5H), 1.57-1.42 (m, 10H), 1.30-1.08 (m, 4H).

Example 368 [5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-2-(6-oxa-2-azaspiro[3.3]heptane-2-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 149 substituting 2-oxa-6-azaspiro[3.3]heptane for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃F₃N₅O₃S, 537.6; m/z found, 538.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.19-8.11 (m, 1H), 6.67-6.58 (m, 1H), 5.01-4.80 (m, 7H), 4.44-4.34 (m, 2H), 4.25-4.08 (m, 1H), 3.65-3.44 (m, 2H), 2.14-2.03 (m, 1H), 2.03-1.90 (m, 1H), 1.84-1.74 (m, 1H), 1.62-1.53 (m, 1H), 1.51-1.40 (s, 9H), 1.29-1.02 (m, 3H).

Example 369 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(trans-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₃S, 525.6; m/z found, 526.2 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.22-8.13 (s, 1H), 7.52-7.38 (m, 1H), 6.66-6.58 (m, 1H), 4.98-4.89 (s, 1H), 4.25-4.00 (m, 3H), 3.63-3.31 (m, 3H), 2.29-2.12 (m, 2H), 2.11-1.98 (m, 1H), 1.95-1.83 (m, 1H), 1.80-1.70 (m, 2H), 1.57-1.41 (m, 10H), 1.29-1.00 (m, 4H).

Example 370 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-((1R*,2R*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: CHIRALPAK AD-H, 5 μm, 250×20 mm, Mobile phase: 85% CO₂, 15% EtOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₄H₃₀F₃N₅O₃S, 525.6; m/z found, 525.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.21-8.12 (s, 1H), 7.52-7.37 (m, 1H), 6.67-6.58 (m, 1H), 4.98-4.87 (m, 1H), 4.26-4.01 (m, 3H), 3.63-3.31 (m, 2H), 2.27-2.13 (m, 2H), 2.10-2.00 (m, 1H), 1.94-1.84 (m, 1H), 1.80-1.69 (m, 2H), 1.57-1.48 (m, 2H), 1.27-1.20 (m, 3H), 1.48-1.43 (m, 9H), 1.07-1.02 (d, J=6.4 Hz, 1H).

Example 371 5-(6-(tert-Butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: CHIRALPAK AD-H, 5 μm, 250×20 mm, Mobile phase: 85% CO₂, 15% EtOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₄H₃₀F₃N₅O₃S, 525.6; m/z found, 525.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.22-8.13 (s, 1H), 7.53-7.38 (m, 1H), 6.67-6.60 (m, 1H), 5.01-4.91 (s, 1H), 4.27-4.00 (m, 3H), 3.62-3.29 (m, 2H), 2.28-2.12 (m, 2H), 2.12-1.97 (m, 1H), 1.97-1.81 (m, 1H), 1.81-1.66 (m, 2H), 1.60-1.48 (m, 2H), 1.48-1.41 (s, 9H), 1.27-1.21 (m, 3H), 1.07-1.02 (d, J=6.4 Hz, 1H).

Example 372 [5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-2-[(3R,4R)-3-fluoro-4-hydroxy-pyrrolidine-1-carbonyl]thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 149 substituting (3R,4R)-4-fluoropyrrolidin-3-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₉F₄N₅O₃S, 543.6; m/z found, 543.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.17-8.08 (m, 1H), 6.70-6.62 (m, 1H), 5.15-4.88 (m, 2H), 4.63-4.31 (m, 3H), 4.24-4.10 (m, 2H), 4.05-3.78 (m, 2H), 1.81-1.70 (m, 1H), 3.62-3.39 (m, 2H), 2.13-2.00 (m, 1H), 1.99-1.83 (m, 1H), 1.49-1.41 (m, 10H), 1.28-1.18 (m, 3H).

Example 373 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-N-[(3R)-tetrahydrofuran-3-yl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-tetrahydrofuran-3-amine for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃F₃N₅O₃S, 525.6; m/z found, 525.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.21-8.15 (s, 1H), 7.41-7.29 (m, 1H), 6.67-6.60 (m, 1H), 5.04-4.97 (m, 1H), 4.77-4.67 (m, 1H), 4.25-4.08 (m, 1H), 4.08-3.98 (m, 1H), 3.98-3.90 (m, 1H), 3.90-3.80 (m, 2H), 3.46-3.29 (m, 1H), 2.44-2.30 (m, 1H), 2.11-1.82 (m, 4H), 1.80-1.68 (m, 1H), 1.58-1.49 (m, 1H), 1.49-1.41 (s, 9H), 1.27-1.04 (m, 3H).

Example 374 5-[6-(tert-Butylamino)-4-(trifluoromethyl)-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-N-tetrahydropyran-4-yl-thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting tetrahydro-2H-pyran-4-amine for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 107) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₂F₃N₅O₃S, 539.6; m/z found, 539.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.21-8.13 (s, 1H), 7.20-7.09 (m, 1H), 6.70-6.63 (m, 1H), 5.19-5.11 (m, 1H), 4.27-4.08 (m, 2H), 4.06-3.98 (m, 2H), 3.59-3.50 (m, 2H), 3.37-3.32 (m, 1H), 2.11-1.98 (m, 4H), 1.94-1.82 (m, 1H), 1.77-1.60 (m, 3H), 1.56-1.48 (m, 1H), 1.48-1.42 (s, 9H), 1.27-1.06 (m, 3H).

Example 375 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-(trans-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 561.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.11-8.01 (m, 1H), 7.47-7.34 (m, 1H), 6.95-6.73 (m, 1H), 4.86-4.72 (m, 2H), 4.32-4.01 (m, 3H), 3.61-3.53 (dd, J=7.9, 6.1 Hz, 1H), 3.49-3.19 (m, 2H), 2.29-2.14 (m, 2H), 2.11-1.83 (m, 3H), 1.83-1.71 (m, 1H), 1.69-1.48 (m, 4H), 1.28-1.17 (m, 3H), 1.09-0.94 (m, 4H).

Example 376 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1R*,2R*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 75% CO₂, 25% i-PrOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 561.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 7.52-7.40 (m, 1H), 6.78-6.75 (m, 1H), 5.09-5.02 (m, 1H), 4.85-4.71 (s, 1H), 4.31-3.99 (m, 3H), 3.60-3.53 (m, 1H), 3.47-3.29 (m, 1H), 2.27-2.15 (m, 2H), 2.09-1.86 (m, 4H), 1.81-1.70 (m, 2H), 1.68-1.48 (m, 3H), 1.27-1.18 (m, 3H), 1.08-0.96 (m, 4H).

Example 377 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 75% CO₂, 25% i-PrOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 561.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.01 (m, 1H), 7.58-7.42 (m, 1H), 6.81-6.73 (m, 1H), 5.25-5.16 (m, 1H), 4.84-4.73 (s, 1H), 4.27-4.07 (m, 3H), 3.60-3.53 (m, 1H), 3.44-3.31 (m, 1H), 2.26-2.14 (m, 2H), 2.08-1.87 (m, 3H), 1.80-1.69 (m, 2H), 1.68-1.48 (m, 3H), 1.27-1.18 (m, 4H), 1.07-0.97 (m, 4H).

Example 378 [5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-2-(8-oxa-3-azabicyclo[3.2.1]octane-3-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 148 substituting 8-oxa-3-azabicyclo[3.2.1]octane for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₆H₃₀F₅N₅O₃S, 587.6; m/z found, 587.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.07-8.02 (m, 1H), 7.28 (s, 1H), 6.81-6.72 (m, 1H), 5.20-5.05 (m, 2H), 4.77 (br s, 1H), 4.52-4.39 (m, 2H), 4.37-4.29 (m, 1H), 4.26-4.17 (m, 1H), 3.62-3.51 (m, 2H), 3.48-3.41 (m, 1H), 3.22 (br d, J=13.2 Hz, 1H), 2.20-1.81 (m, 8H), 1.84-1.77 (m, 1H), 1.68-1.53 (m, 2H), 1.29-1.20 (m, 2H), 1.06-0.98 (m, 3H).

Example 379 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-(cis-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 561.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-8.00 (m, 1H), 7.83-7.75 (m, 1H), 6.81-6.74 (m, 1H), 4.85-4.72 (m, 2H), 4.63-4.49 (m, 2H), 4.40-4.16 (m, 1H), 3.63-3.36 (m, 2H), 2.57-2.44 (m, 1H), 2.36-2.14 (m, 3H), 2.11-1.84 (m, 4H), 1.82-1.73 (m, 1H), 1.69-1.50 (m, 3H), 1.24-1.20 (m, 2H), 1.08-1.02 (m, 4H).

Example 380 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1S*,2R*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Chiralpak AS-H, 5 μm, 250×20 mm, Mobile phase: 90% CO₂, 10% MeOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 561.8 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-7.99 (m, 1H), 7.98-7.90 (m, 1H), 6.82-6.72 (m, 1H), 5.40-5.27 (m, 1H), 4.86-4.71 (m, 1H), 4.60-4.47 (m, 2H), 4.36-4.08 (m, 1H), 3.63-3.30 (m, 3H), 2.32-2.12 (m, 3H), 2.08-1.83 (m, 4H), 1.81-1.71 (m, 1H), 1.68-1.57 (m, 1H), 1.28-1.13 (m, 4H), 1.10-0.96 (m, 4H).

Example 381 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1R*,2S*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Chiralpak AS-H, 5 μm, 250×20 mm, Mobile phase: 90% CO₂, 10% MeOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 561.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-8.00 (m, 1H), 7.99-7.91 (m, 1H), 6.86-6.71 (m, 1H), 5.51-5.37 (m, 1H), 4.86-4.72 (m, 1H), 4.58-4.46 (m, 2H), 4.40-4.08 (m, 1H), 3.72-3.30 (m, 3H), 2.34-2.11 (m, 2H), 2.09-1.83 (m, 4H), 1.81-1.70 (m, 1H), 1.70-1.57 (m, 1H), 1.57-1.47 (m, 1H), 1.28-1.13 (m, 4H), 1.10-0.96 (m, 4H).

Example 382 N-(1-Acetylazetidin-3-yl)-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting 1-(3-aminoazetidin-1-yl)ethan-1-one HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₉F₅N₆O₃S, 588.6; m/z found, 588.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.74-7.62 (m, 1H), 6.93-6.65 (m, 2H), 5.25-5.15 (m, 1H), 4.92-4.74 (m, 2H), 4.57-4.51 (m, 1H), 4.46-4.38 (m, 1H), 4.26-3.99 (m, 3H), 3.61-3.31 (m, 2H), 2.10-1.93 (m, 3H), 1.93-1.90 (s, 3H), 1.82-1.73 (m, 1H), 1.68-1.51 (m, 2H), 1.26-1.17 (m, 2H), 1.08-0.96 (m, 4H).

Example 383 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-N-(1-methylsulfonylazetidin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 1-(methylsulfonyl)azetidin-3-amine for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₉F₅N₆O₄S₂, 624.8; m/z found, 624.8 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.68-7.59 (m, 1H), 6.80-6.73 (m, 2H), 5.07-4.98 (m, 1H), 4.92-4.73 (m, 2H), 4.26-4.17 (m, 3H), 4.16-4.08 (m, 2H), 3.62-3.31 (m, 2H), 2.98-2.93 (m, 3H), 2.11-2.01 (m, 1H), 2.01-1.88 (m, 2H), 1.83-1.74 (m, 1H), 1.69-1.52 (m, 2H), 1.28-1.21 (m, 2H), 1.07-0.97 (m, 4H).

Example 384 [5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-2-(6-oxa-2-azaspiro[3.3]heptane-2-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 149 substituting 2-oxa-6-azaspiro[3.3]heptane hemioxalate for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.6; m/z found, 573.9 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.06-7.98 (m, 1H), 6.78-6.73 (m, 1H), 5.11-5.03 (m, 1H), 4.91-4.73 (m, 7H), 4.42-4.37 (m, 2H), 4.26-4.18 (m, 1H), 3.62-3.44 (m, 2H), 2.13-2.03 (m, 1H), 2.00-1.92 (m, 2H), 1.90-1.75 (m, 2H), 1.71-1.54 (m, 2H), 1.28-1.22 (m, 2H), 1.06-0.97 (m, 4H).

Example 385 [5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-2-(3-oxa-6-azaspiro[3.3]heptane-6-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 149 substituting 1-oxa-6-azaspiro[3.3]heptane hemioxalate for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.6; m/z found, 573.9 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.05-7.98 (m, 1H), 6.78-6.72 (m, 1H), 5.21-5.09 (m, 1H), 4.93-4.73 (m, 3H), 4.63-4.53 (m, 2H), 4.47-4.41 (m, 2H), 4.27-4.15 (m, 1H), 3.70-3.41 (m, 2H), 2.98-2.89 (m, 2H), 2.13-2.03 (m, 1H), 2.01-1.75 (m, 4H), 1.73-1.52 (m, 2H), 1.28-1.19 (m, 2H), 1.06-0.92 (m, 4H).

Example 386 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-(trans-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 547.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.11-8.02 (m, 1H), 7.44-7.32 (m, 1H), 6.79-6.70 (m, 1H), 5.00-4.85 (m, 2H), 4.32-4.02 (m, 3H), 3.62-3.31 (m, 2H), 3.25-3.15 (m, 1H), 2.28-2.15 (m, 2H), 2.10-2.00 (m, 1H), 1.97-1.86 (m, 1H), 1.82-1.72 (m, 1H), 1.68-1.61 (m, 2H), 1.60-1.49 (m, 1H), 1.44-1.39 (m, 3H), 1.29-1.20 (m, 3H), 1.02-0.96 (m, 1H).

Example 387 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1R*,2R*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 75% CO₂, 25% i-PrOH). MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 547.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.11-8.00 (m, 1H), 7.49-7.36 (m, 1H), 6.77-6.68 (d, J=14.9 Hz, 1H), 5.23-5.11 (m, 1H), 5.02-4.87 (m, 1H), 4.35-4.12 (m, 2H), 4.13-4.03 (m, 1H), 3.61-3.53 (m, 1H), 3.53-3.43 (m, 1H), 3.41-3.30 (m, 1H), 2.27-2.14 (m, 2H), 2.10-1.98 (m, 1H), 1.98-1.83 (m, 2H), 1.82-1.71 (m, 2H), 1.68-1.49 (m, 2H), 1.44-1.36 (m, 3H), 1.26-1.21 (m, 2H), 1.01-0.95 (d, J=6.4 Hz, 1H).

Example 388 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 75% CO₂, 25% i-PrOH). MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 547.8 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.57-7.44 (m, 1H), 6.76-6.66 (m, 1H), 5.60-5.43 (m, 1H), 5.03-4.85 (m, 1H), 4.32-4.08 (m, 3H), 3.62-3.52 (m, 1H), 3.52-3.42 (m, 1H), 3.42-3.31 (m, 1H), 2.28-2.12 (m, 2H), 2.11-1.98 (m, 1H), 1.98-1.83 (m, 1H), 1.83-1.68 (m, 2H), 1.69-1.47 (m, 2H), 1.44-1.36 (m, 3H), 1.27-1.17 (m, 3H), 1.03-0.96 (m, 1H).

Example 389 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-(cis-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 547.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.02 (m, 1H), 7.82-7.72 (m, 1H), 6.79-6.71 (m, 1H), 5.00-4.81 (m, 2H), 4.64-4.50 (m, 2H), 4.25-4.15 (m, 1H), 3.63-3.38 (m, 2H), 2.45-2.35 (m, 1H), 2.33-2.25 (m, 1H), 2.22-2.13 (m, 1H), 2.06-1.91 (m, 2H), 1.83-1.72 (m, 1H), 1.61-1.52 (m, 3H), 1.44-1.38 (d, J=6.7 Hz, 3H), 1.27-1.21 (m, 3H), 1.09-1.04 (m, 1H).

Example 390 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1S*,2R*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 75% CO₂, 25% i-PrOH). MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 547.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.08-8.00 (m, 1H), 7.96-7.89 (d, J=6.7 Hz, 1H), 6.74-6.66 (m, 1H), 5.61-5.45 (m, 1H), 5.02-4.87 (m, 1H), 4.57-4.35 (m, 2H), 4.23-3.98 (m, 1H), 3.60-3.49 (m, 1H), 3.44-3.35 (m, 1H), 2.34-2.12 (m, 3H), 2.10-1.86 (m, 4H), 1.79-1.71 (m, 1H), 1.68-1.49 (m, 1H), 1.42-1.35 (m, 3H), 1.28-1.17 (m, 3H), 1.09-1.00 (d, J=6.4 Hz, 1H).

Example 391 5-(4-(Difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-N-((1R*,2S*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting cis-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 75% CO₂, 25% i-PrOH). MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₃S, 547.5; m/z found, 547.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-8.00 (m, 1H), 7.97-7.88 (m, 1H), 6.75-6.67 (m, 1H), 5.53-5.38 (m, 1H), 5.03-4.86 (m, 1H), 4.60-4.46 (m, 2H), 4.40-4.13 (m, 1H), 3.63-3.47 (m, 1H), 3.46-3.36 (m, 1H), 2.33-2.20 (m, 2H), 2.20-2.11 (m, 1H), 2.09-1.81 (m, 4H), 1.81-1.62 (m, 1H), 1.59-1.48 (m, 1H), 1.43-1.36 (m, 3H), 1.27-1.18 (m, 3H), 1.10-1.02 (d, J=6.4 Hz, 1H).

Example 392 [5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-2-(6-oxa-3-azabicyclo[3.1.1]heptane-3-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 149 substituting 6-oxa-3-azabicyclo[3.1.1]heptane TsOH for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.6; m/z found, 573.9 [M+H]⁺. ¹HNMR (600 MHz, CDCl₃) δ 8.09-8.00 (m, 1H), 6.81-6.74 (m, 1H), 5.54-5.42 (m, 1H), 4.85-4.59 (m, 4H), 4.44-4.33 (m, 1H), 4.32-4.17 (m, 1H), 4.16-4.04 (m, 1H), 3.94-3.86 (m, 1H), 3.66-3.55 (m, 1H), 3.54-3.42 (m, 1H), 3.36-3.27 (m, 1H), 2.11-2.02 (m, 1H), 2.00-1.84 (m, 4H), 1.83-1.74 (m, 1H), 1.71-1.52 (m, 2H), 1.29-1.19 (m, 2H), 1.08-0.93 (m, 4H).

Example 393 [5-[4-(Difluoromethyl)-6-[[(1S)-1-(tifluoromethyl)propyl]amino]-3-pyridyl]-2-(3-methylsulfonylazetidine-1-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

To a 25 mL round bottomed flask was added ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (0.25 g, 0.48 mmol, Intermediate 104: Step B), DIPEA (0.3 mL, 1.7 mmol), water (2 mL) and EtOH (2 mL) and the reaction was stirred at 80° C. for 2.5 h. The contents were cooled to room temperature and the pH was adjusted to approximately 4 with 1 M aqueous hydrochloric acid. The mixture was then extracted three times with ethyl acetate and the combined organic phases were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude material was then taken up into DCM (5 mL), cooled to 0° C., then oxalyl chloride (60 μL, 0.67 mmol) and DMF (8 uL) were added under a nitrogen atmosphere. The reaction solution was stirred at 0° C. for 25 minutes, then warmed to room temperature and stirred for 45 minutes. The reaction solution was then concentrated under reduced pressure. The crude material was then re-dissolved in DCM (5 mL) then cooled to 0° C. under a nitrogen atmosphere followed by the addition of 3-methylsulfonylazetidine (78.7 mg, 0.58 mmol) and DIPEA (0.23 mL, 1.4 mmol). The contents were allowed to stir at 0° C. for 5 minutes then the contents were warmed to room temperature and stirred for 3 days. The reaction solution was then re-cooled to 0° C., quenched with a saturated aqueous ammonium chloride solution. The contents were transferred to a separatory funnel and extracted three times with ethyl acetate and the combined organic phases were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue was dissolved in chloroform and purified by FCC (0-100% EtOAc/Hexanes) to provide the title compound. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₄S₂, 609.6; m/z found, 609.8 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.07-7.99 (m, 1H), 6.80-6.71 (m, 1H), 5.22-5.14 (m, 1H), 5.11-4.94 (m, 2H), 4.85-4.72 (m, 1H), 4.59-4.49 (m, 2H), 4.23-4.09 (m, 2H), 3.61-3.49 (m, 1H), 3.47-3.39 (m, 1H), 2.99-2.93 (m, 3H), 2.12-2.01 (m, 1H), 2.00-1.89 (m, 2H), 1.86-1.74 (m, 1H), 1.69-1.49 (m, 2H), 1.27-1.16 (m, 3H), 1.07-0.94 (m, 4H).

Example 394 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-N-tetrahydropyran-4-yl-thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting tetrahydro-2H-pyran-4-amine for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 575.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.10-8.00 (m, 1H), 7.16-7.04 (m, 1H), 6.82-6.75 (m, 1H), 5.34-5.24 (m, 1H), 4.86-4.74 (m, 1H), 4.28-4.13 (m, 2H), 4.06-3.97 (m, 2H), 3.59-3.51 (m, 3H), 3.45-3.31 (m, 1H), 2.09-1.85 (m, 6H), 1.81-1.72 (m, 1H), 1.71-1.49 (m, 4H), 1.24-1.19 (m, 2H), 1.07-1.00 (m, 4H).

Example 395 [5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-2-(morpholine-4-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 148 substituting morpholine for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₈F₅N₅O₃S, 561.6; m/z found, 561.9 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.08-8.00 (m, 1H), 6.80-6.72 (m, 1H), 5.23-5.11 (m, 1H), 4.84-4.71 (m, 1H), 4.52-4.27 (m, 2H), 4.25-4.16 (m, 1H), 3.89-3.74 (m, 6H), 3.64-3.39 (m, 2H), 2.10-2.01 (m, 1H), 2.01-1.83 (m, 3H), 1.82-1.73 (m, 1H), 1.69-1.50 (m, 2H), 1.23-1.20 (m, 2H), 1.06-0.99 (m, 4H).

Example 396 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1S,2S)-2-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1S,2S)-2-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.6; m/z found, 522.0 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-7.99 (m, 1H), 7.35-7.23 (m, 1H), 6.75-6.62 (m, 1H), 5.01-4.92 (m, 1H), 4.26-4.11 (m, 2H), 4.09-4.00 (m, 1H), 4.00-3.92 (s, 1H), 3.63-3.51 (m, 1H), 3.38-3.27 (m, 1H), 2.33-2.21 (m, 1H), 2.13-1.98 (m, 2H), 1.99-1.81 (m, 3H), 1.81-1.69 (m, 3H), 1.67-1.57 (m, 1H), 1.57-1.48 (m, 1H), 1.48-1.43 (s, 9H), 1.24-1.18 (m, 2H), 1.03-0.96 (m, 1H).

Example 397 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1R,2R)-2-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,2R)-2-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.6; m/z found, 522.0 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.09-7.97 (m, 1H), 7.36-7.25 (m, 1H), 6.74-6.62 (m, 1H), 5.03-4.93 (m, 1H), 4.26-4.10 (m, 2H), 4.10-4.01 (m, 1H), 4.02-3.95 (s, 1H), 3.61-3.52 (m, 1H), 3.38-3.27 (m, 1H), 2.32-2.21 (m, 1H), 2.13-2.00 (m, 2H), 1.98-1.81 (m, 3H), 1.81-1.67 (m, 3H), 1.67-1.57 (m, 1H), 1.57-1.48 (m, 1H), 1.48-1.42 (m, 9H), 1.24-1.19 (m, 2H), 1.03-0.96 (m, 1H).

Example 398 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1S,3S)-3-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1S,3S)-3-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 575.9 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.09-8.00 (m, 1H), 7.22-7.08 (m, 1H), 6.82-6.74 (m, 1H), 5.19-5.09 (m, 1H), 4.84-4.73 (s, 1H), 4.69-4.58 (m, 1H), 4.53-4.44 (m, 1H), 4.26-4.15 (m, 1H), 3.62-3.51 (m, 1H), 3.42-3.28 (m, 1H), 2.42-2.31 (m, 1H), 2.23-2.01 (m, 4H), 2.01-1.67 (m, 6H), 1.67-1.47 (m, 3H), 1.29-1.18 (m, 2H), 1.07-0.96 (m, 4H).

Example 399 5-[4-(Difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R,3R)-3-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,3R)-3-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 102) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 575.9 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.09-8.00 (m, 1H), 7.22-7.11 (m, 1H), 6.83-6.73 (m, 1H), 5.23-5.16 (m, 1H), 4.86-4.72 (s, 1H), 4.69-4.58 (m, 1H), 4.53-4.44 (m, 1H), 4.26-4.09 (m, 1H), 3.61-3.52 (m, 1H), 3.42-3.27 (m, 1H), 2.42-2.30 (m, 1H), 2.27-2.15 (m, 2H), 2.15-2.01 (m, 2H), 2.01-1.67 (m, 6H), 1.67-1.47 (m, 3H), 1.29-1.18 (m, 2H), 1.07-0.97 (m, 4H).

Example 400 5-(6-(tert-Butylamino)-4-(difluoromethyl)pyridin-3-yl)-N-((1R,3S)-3-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,3R)-3-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₁F₂N₅O₃S, 507.6; m/z found, 507.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.06-7.98 (m, 1H), 7.49-7.36 (m, 1H), 6.76-6.62 (m, 1H), 5.11-5.01 (s, 1H), 4.71-4.51 (m, 2H), 4.30-4.07 (m, 1H), 3.64-3.52 (m, 1H), 3.40-3.11 (m, 2H), 2.53-2.36 (m, 4H), 2.13-1.99 (m, 1H), 1.99-1.82 (m, 2H), 1.82-1.68 (m, 1H), 1.68-1.49 (m, 1H), 1.49-1.41 (d, J=9.1 Hz, 9H), 1.32-1.17 (m, 2H), 1.04-0.93 (d, J=6.4 Hz, 1H).

Example 401 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(3S,4R)-4-hydroxytetrahydrofuran-3-yl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3R,4S)-4-aminotetrahydrofuran-3-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₁F₂N₅O₄S, 523.6; m/z found, 523.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.08-7.97 (m, 1H), 7.47-7.33 (m, 1H), 6.75-6.60 (m, 1H), 5.05-4.96 (d, J=2.1 Hz, 1H), 4.48-4.37 (m, 2H), 4.27-4.08 (m, 3H), 4.08-3.97 (s, 1H), 3.90-3.83 (m, 1H), 3.80-3.73 (m, 1H), 3.63-3.53 (m, 1H), 3.44-3.25 (m, 1H), 2.11-1.98 (m, 1H), 1.96-1.83 (m, 1H), 1.81-1.69 (m, 1H), 1.67-1.50 (m, 1H), 1.50-1.42 (s, 9H), 1.27-1.22 (m, 3H), 1.01-0.93 (d, J=6.4 Hz, 1H).

Example 402 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(3R,4S)-4-hydroxytetrahydrofuran-3-yl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (3S,4R)-4-aminotetrahydrofuran-3-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₁F₂N₅O₄S, 523.6; m/z found, 523.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.07-7.98 (m, 1H), 7.47-7.36 (m, 1H), 6.76-6.59 (m, 1H), 5.05-4.96 (s, 1H), 4.48-4.37 (m, 2H), 4.26-4.09 (m, 3H), 4.09-4.00 (s, 1H), 3.90-3.82 (m, 1H), 3.81-3.73 (m, 1H), 3.62-3.52 (m, 1H), 3.38-3.26 (m, 1H), 2.11-2.00 (m, 1H), 1.99-1.82 (m, 1H), 1.82-1.70 (m, 1H), 1.59-1.49 (m, 1H), 1.49-1.42 (m, 9H), 1.31-1.18 (m, 3H), 1.02-0.96 (d, J=6.4 Hz, 1H).

Example 403 5-(6-(tert-Butylamino)-4-(difluoromethyl)pyridin-3-yl)-N-((1R*,2R*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 65% CO₂, 35% i-PrOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₄H₃₁F₂N₅O₃S, 507.6; m/z found, 507.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.07-7.98 (m, 1H), 7.57-7.42 (m, 1H), 6.75-6.60 (m, 1H), 5.00-4.88 (s, 1H), 4.27-3.95 (m, 3H), 3.63-3.52 (m, 1H), 3.43-3.26 (m, 1H), 2.28-2.12 (m, 2H), 2.11-1.99 (m, 1H), 1.99-1.82 (m, 1H), 1.81-1.67 (m, 1H), 1.67-1.49 (m, 2H), 1.48-1.42 (s, 9H), 1.25-1.17 (m, 5H), 1.00-0.94 (d, J=6.4 Hz, 1H).

Example 404 5-(6-(tert-Butylamino)-4-(difluoromethyl)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclobutyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 65% CO₂, 35% i-PrOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₄H₃₁F₂N₅O₃S, 507.6; m/z found, 508.0 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.08-7.97 (m, 1H), 7.57-7.42 (m, 1H), 6.78-6.59 (m, 1H), 4.99-4.89 (s, 1H), 4.28-4.03 (m, 3H), 3.62-3.52 (m, 1H), 3.42-3.29 (m, 1H), 2.28-2.11 (m, 2H), 2.11-1.99 (m, 1H), 1.96-1.83 (m, 2H), 1.81-1.68 (m, 2H), 1.59-1.49 (m, 2H), 1.49-1.41 (s, 9H), 1.28-1.17 (m, 3H), 1.01-0.95 (d, J=6.4 Hz, 1H).

Example 405 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1R*,2R*)-2-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 70% CO₂, 30% i-PrOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.6; m/z found, 573.8 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.13-8.04 (s, 1H), 7.59-7.48 (d, J=5.4 Hz, 1H), 6.82-6.74 (m, 1H), 5.18-5.09 (d, J=9.7 Hz, 1H), 4.86-4.72 (m, 1H), 4.70-4.61 (m, 1H), 4.21-4.05 (m, 3H), 2.28-2.11 (m, 2H), 2.03-1.89 (m, 1H), 1.81-1.67 (m, 3H), 1.67-1.55 (m, 2H), 1.55-1.37 (m, 7H), 1.23-1.17 (m, 1H), 1.07-0.99 (m, 3H).

Example 406 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting trans-2-aminocyclobutan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 99) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate followed by SFC purification (Stationary phase: Lux amylose 2, 5 μm, 250×21.2 mm, Mobile phase: 70% CO₂, 30% i-PrOH (0.3% i-PrNH₂)). MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.6; m/z found, 573.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.11-8.06 (s, 1H), 7.52-7.45 (d, J=5.2 Hz, 1H), 6.79-6.75 (m, 1H), 5.03-4.95 (d, J=9.7 Hz, 1H), 4.85-4.73 (m, 1H), 4.71-4.62 (m, 1H), 4.22-4.04 (m, 3H), 2.28-2.13 (m, 2H), 2.04-1.91 (m, 1H), 1.81-1.68 (m, 3H), 1.68-1.55 (m, 2H), 1.54-1.37 (m, 7H), 1.23-1.18 (m, 1H), 1.08-0.99 (m, 3H).

Example 407 5-[4-(Difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1S)-1-(hydroxymethyl)propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (S)-2-aminobutan-1-ol for (R)-(−)-2-amino-1-propanol and 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₈F₅N₅O₃S, 549.6; m/z found, 549.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.10-7.99 (m, 1H), 7.45-7.33 (m, 1H), 6.71 (s, 1H), 5.64-5.50 (m, 1H), 5.02-4.87 (m, 1H), 4.38-4.12 (m, 1H), 4.09-3.99 (m, 1H), 3.82-3.67 (m, 2H), 3.63-3.32 (m, 2H), 3.25-2.90 (m, 1H), 2.69-2.14 (m, 1H), 2.12-1.97 (m, 1H), 1.97-1.82 (m, 1H), 1.82-1.60 (m, 3H), 1.60-1.48 (m, 1H), 1.43-1.34 (m, 3H), 1.23 (d, J=6.3 Hz, 2H), 1.08-0.96 (m, 4H).

Example 408 5-[4-(Difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1R)-1-(hydroxymethyl)propyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (R)-2-aminobutan-1-ol for (R)-(−)-2-amino-1-propanol and 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₈F₅N₅O₃S, 549.6; m/z found, 549.9 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.08 (s, 1H), 7.42-7.30 (m, 1H), 6.71 (s, 1H), 5.54-5.40 (m, 1H), 5.03-4.86 (m, 1H), 4.32-4.14 (m, 1H), 4.10-3.99 (m, 1H), 3.84-3.68 (m, 2H), 3.64-3.33 (m, 2H), 3.08-2.85 (m, 1H), 2.43-2.11 (m, 1H), 2.11-1.83 (m, 2H), 1.83-1.61 (m, 3H), 1.59-1.48 (m, 1H), 1.43-1.37 (m, 3H), 1.25-1.20 (m, 2H), 1.02 (s, 4H), 1.09-0.98 (m, 4H).

Example 409 5-[4-(Difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-N-(1-methylsulfonylazetidin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting 1-(methylsulfonyl)azetidin-3-amine for (R)-(−)-2-amino-1-propanol and ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₇F₅N₆O₄S₂, 610.6; m/z found, 610.8 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09-8.07 (m, 1H), 7.66-7.54 (m, 1H), 6.77-6.68 (m, 1H), 5.19-5.06 (m, 1H), 5.03-4.82 (m, 2H), 4.36-4.17 (m, 3H), 4.18-4.08 (m, 2H), 3.63-3.48 (m, 1H), 3.44-3.30 (m, 1H), 2.96 (s, 3H), 2.05 (s, 1H), 2.00-1.88 (m, 1H), 1.86-1.72 (m, 1H), 1.72-1.47 (m, 2H), 1.47-1.37 (m, 3H), 1.26 (s, 2H), 1.04-0.95 (m, 1H).

Example 410 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1R,3R)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 149 substituting (1R,3R)-3-aminocyclopentan-1-ol HCl for 3-hydroxy-3-methylazetidine HCl and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 96) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₆F₇N₅O₃S, 597.6; m/z found, 597.8 [M+H]⁺. ¹HNMR (500 MHz, CDCl₃) δ 8.07-8.02 (m, 1H), 7.08-7.03 (m, 1H), 6.64 (br s, 1H), 5.20 (d, J=9.3 Hz, 1H), 4.95 (br dd, J=7.3, 15.8 Hz, 1H), 4.67-4.61 (m, 1H), 4.54-4.46 (m, 2H), 4.03 (br d, J=13.2 Hz, 1H), 3.89-3.81 (m, 1H), 2.61-2.52 (m, 1H), 2.43-2.35 (m, 1H), 2.24-2.08 (m, 5H), 1.96 (br s, 1H), 1.86-1.80 (m, 1H), 1.76-1.68 (m, 1H), 1.66-1.58 (m, 1H), 1.42-1.39 (m, 3H), 1.38-1.34 (m, 2H).

Example 411 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1S,3S)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 153) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,3S)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.6; m/z found, 574.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.83 (d, J=8.2 Hz, 1H), 8.03 (s, 1H), 7.77 (d, J=8.8 Hz, 1H), 7.13-6.82 (m, 2H), 5.06-4.95 (m, 1H), 4.51 (d, J=3.5 Hz, 1H), 4.47-4.37 (m, 2H), 4.21-4.14 (m, 1H), 4.03-3.97 (m, 1H), 2.05-1.86 (m, 2H), 1.82-1.72 (m, 2H), 1.61-1.51 (m, 1H), 1.48-1.35 (m, 5H), 1.33-1.26 (m, 6H), 1.21-1.11 (m, 1H).

Example 412 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]-N-tetrahydropyran-4-yl-thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting tetrahydro-2H-pyran-4-amine for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 106) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.6; m/z found, 522.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.03-8.71 (m, 1H), 7.99-7.91 (m, 1H), 7.11-6.73 (m, 3H), 4.17-3.92 (m, 2H), 3.84 (d, J=10.8 Hz, 2H), 3.38-3.33 (m, 2H), 3.27-3.23 (m, 1H), 2.06-1.86 (m, 1H), 1.85-1.71 (m, 2H), 1.70-1.58 (m, 4H), 1.57-1.40 (m, 2H), 1.36 (s, 9H), 1.05 (d, J=6.4 Hz, 2H), 0.83 (d, J=6.4 Hz, 1H).

Example 413 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-(tert-butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1S,3S)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 155) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,3S)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₃S, 533.6; m/z found, 534.1 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.83 (d, J=7.7 Hz, 1H), 7.94 (s, 1H), 7.13-6.73 (m, 3H), 4.60-4.38 (m, 3H), 4.24-4.14 (m, 1H), 3.99-3.84 (m, 1H), 2.03-1.89 (m, 2H), 1.82-1.71 (m, 2H), 1.63-1.51 (m, 1H), 1.44-1.24 (m, 16H), 1.22-1.09 (m, 2H).

Example 414 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1S,3S)-3-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 156) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,3S)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.6; m/z found, 522.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.80 (d, J=8.2 Hz, 1H), 7.95 (s, 1H), 7.12-6.70 (m, 3H), 4.56-4.48 (m, 1H), 4.48-4.35 (m, 1H), 4.22-4.10 (m, 1H), 4.03-3.93 (m, 1H), 3.26-3.20 (m, 1H), 2.06-1.85 (m, 3H), 1.85-1.67 (m, 4H), 1.65-1.50 (m, 2H), 1.48-1.40 (m, 2H), 1.36 (s, 9H), 1.04 (d, J=6.2 Hz, 2H), 0.83 (d, J=6.4 Hz, 1H).

Example 415 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1S,3S)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 157) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,3S)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₄H₂₆F₇N₅O₃S, 597.6; m/z found, 597.9 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.44 (br s, 1H), 8.08 (s, 1H), 7.54 (d, J=8.5 Hz, 1H), 7.05-6.73 (m, 2H), 5.09-4.97 (m, 1H), 4.51-4.42 (m, 1H), 4.33-4.23 (m, 2H), 4.12-3.88 (m, 2H), 2.69-2.54 (m, 1H), 2.21-1.78 (m, 6H), 1.70-1.47 (m, 2H), 1.36 (d, J=7.0 Hz, 3H), 1.22 (s, 3H).

Example 416 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1S,3S)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 159) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,3S)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₅H₂₈F₇N₅O₃S, 611.6; m/z found, 612.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.84 (d, J=8.3 Hz, 1H), 8.06 (s, 1H), 7.75-7.65 (m, 1H), 7.12-6.75 (m, 2H), 4.91-4.79 (m, 1H), 4.56 (d, J=3.8 Hz, 1H), 4.52-4.41 (m, 1H), 4.38-3.80 (m, 4H), 2.68-2.54 (m, 2H), 2.26-1.74 (m, 6H), 1.67-1.43 (m, 3H), 1.26-1.15 (m, 2H), 1.06-1.02 (m, 1H), 0.95 (t, J=7.4 Hz, 3H).

Example 417 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-[[(1S)-1-cyclopropyl-2,2,2-trifluoro-ethyl]amino]-4-(difluoromethyl)-3-pyridyl]-N-[(3S,4R)-4-hydroxytetrahydrofuran-3-yl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 165) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (3R,4S)-4-aminotetrahydrofuran-3-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₆H₂₈F₅N₅O₄S, 601.6; m/z found, 601.9 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.05-8.96 (m, 1H), 8.03 (s, 1H), 7.90 (d, J=9.0 Hz, 1H), 7.16-6.87 (m, 2H), 5.36-5.30 (m, 1H), 4.56-4.48 (m, 1H), 4.47-4.41 (m, 1H), 4.36-4.30 (m, 1H), 4.23-4.17 (m, 1H), 4.08-3.85 (m, 3H), 3.71-3.63 (m, 1H), 3.56-3.49 (m, 1H), 1.58-1.01 (m, 9H), 0.69-0.59 (m, 1H), 0.57-0.42 (m, 2H), 0.35-0.25 (m, 1H).

Example 418 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1S,2S)-2-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 157) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,2S)-2-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₄H₂₆F₇N₅O₃S, 597.6; m/z found, 598.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.79-8.69 (m, 1H), 8.09 (s, 1H), 7.81-7.74 (m, 1H), 7.13-6.78 (m, 2H), 5.10-4.98 (m, 1H), 4.87-4.82 (m, 1H), 4.74-4.26 (m, 1H), 4.23-3.80 (m, 4H), 2.70-2.56 (m, 1H), 2.35-2.07 (m, 1H), 2.04-1.82 (m, 2H), 1.73-1.42 (m, 4H), 1.34 (d, J=7.0 Hz, 3H), 1.22 (d, J=6.3 Hz, 2H), 1.11-1.01 (m, 1H).

Example 419 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1S,2S)-2-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 159) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,2S)-2-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₅H₂₈F₇N₅O₃S, 611.6; m/z found, 611.9 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.77-8.68 (m, 1H), 8.03 (s, 1H), 7.74-7.63 (m, 1H), 7.10-6.74 (m, 1H), 4.89-4.76 (m, 2H), 4.89-4.76 (m, 2H), 4.36-4.22 (m, 1H), 4.18-4.01 (m, 2H), 4.00-3.78 (m, 2H), 2.65-2.52 (m, 1H), 2.24-2.02 (m, 1H), 2.00-1.90 (m, 1H), 1.89-1.75 (m, 1H), 1.70-1.50 (m, 4H), 1.49-1.38 (m, 1H), 1.25-1.14 (m, 2H), 1.05-0.98 (m, 1H), 0.97-0.85 (m, 3H).

Example 420 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1R,2R)-2-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 157) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1R,2R)-2-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₄H₂₆F₇N₅O₃S, 597.6; m/z found, 597.9 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.79-8.71 (m, 1H), 8.09 (s, 1H), 7.80-7.73 (m, 1H), 7.12-6.77 (m, 2H), 5.10-4.97 (m, 1H), 4.73-4.26 (m, 1H), 4.20-4.05 (m, 2H), 4.04-3.80 (m, 3H), 2.66-2.56 (m, 1H), 2.31-2.06 (m, 1H), 2.04-1.83 (m, 2H), 1.72-1.54 (m, 3H), 1.54-1.43 (m, 1H), 1.34 (d, J=6.5 Hz, 3H), 1.22 (d, J=6.0 Hz, 2H), 1.07 (d, J=6.0 Hz, 1H).

Example 421 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-(1,1-dioxothian-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 157) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid. MS (ESI): mass calcd. for C₂₄H₂₆F₇N₅O₄S₂, 645.6; m/z found, 645.9 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.01-8.93 (m, 1H), 8.04 (s, 1H), 7.78-7.70 (m, 1H), 7.08-6.73 (m, 2H), 5.07-4.61 (m, 1H), 4.34-4.07 (m, 3H), 4.00-3.72 (m, 1H), 3.40-3.36 (m, 1H), 3.12-3.00 (m, 2H), 2.62-2.51 (m, 1H), 2.28-2.14 (m, 3H), 2.13-2.00 (m, 3H), 1.30 (d, J=6.8 Hz, 3H), 1.18 (d, J=6.2 Hz, 2H), 1.02 (d, J=6.2 Hz, 1H).

Example 422 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-tetrahydropyran-4-yl-thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting tetrahydro-2H-pyran-4-amine for (R)-(−)-2-amino-1-propanol and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 158) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₅H₂₈F₇N₅O₃S, 611.6; m/z found, 612.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.90-8.84 (m, 1H), 8.07 (s, 1H), 7.75-7.68 (m, 1H), 7.13-6.79 (m, 2H), 4.94-4.61 (m, 1H), 4.36-4.26 (m, 1H), 4.19-3.78 (m, 5H), 3.43-3.38 (m, 2H), 2.65-2.55 (m, 1H), 2.30-2.06 (m, 1H), 1.88-1.57 (m, 6H), 1.21 (d, J=6.5 Hz, 2H), 1.05 (d, J=6.0 Hz, 1H), 0.96 (t, J=7.3 Hz, 3H).

Example 423 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R)-2-hydroxy-1-methyl-ethyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 158) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₆F₇N₅O₃S, 585.5; m/z found, 586.0 [M+H]⁺. ¹HNMR (400 MHz, DMSO-d₆) δ 8.57-8.47 (m, 1H), 8.07 (s, 1H), 7.76-7.68 (m, 1H), 7.12-6.79 (m, 2H), 4.94-4.60 (m, 2H), 4.37-4.26 (m, 1H), 4.16-3.80 (m, 3H), 3.55-3.39 (m, 2H), 2.66-2.56 (m, 1H), 2.28-2.06 (m, 1H), 1.91-1.78 (m, 1H), 1.69-1.54 (m, 1H), 1.26-1.14 (m, 5H), 1.08 (d, J=6.5 Hz, 1H), 0.96 (t, J=7.3 Hz, 3H).

Example 424 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R,3R)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 159) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1R,3R)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₅H₂₈F₇N₅O₃S, 611.6; m/z found, 612.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.80 (d, J=8.4 Hz, 1H), 8.01 (s, 1H), 7.70-7.63 (m, 1H), 7.07-6.72 (m, 2H), 4.88-4.73 (m, 1H), 4.67-4.49 (m, 1H), 4.48-4.36 (m, 1H), 4.30-4.21 (m, 1H), 4.21-4.13 (m, 1H), 4.13-3.98 (m, 1H), 3.95-3.73 (m, 1H), 2.59-2.50 (m, 1H), 2.24-1.85 (m, 3H), 1.84-1.69 (m, 3H), 1.64-1.38 (m, 3H), 1.15 (d, J=6.4 Hz, 2H), 0.99 (d, J=6.4 Hz, 1H), 0.90 (t, J=7.3 Hz, 3H).

Example 425 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-[(1R,2R)-2-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 159) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1R,2R)-2-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₅H₂₈F₇N₅O₃S, 611.6; m/z found, 611.9 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.77-8.70 (m, 1H), 8.01 (s, 1H), 7.70-7.63 (m, 1H), 7.07-6.73 (m, 2H), 4.86-4.55 (m, 2H), 4.30-4.21 (m, 1H), 4.13-3.99 (m, 2H), 3.98-3.76 (m, 2H), 2.59-2.51 (m, 1H), 2.24-2.00 (m, 1H), 1.98-1.73 (m, 3H), 1.67-1.48 (m, 4H), 1.47-1.36 (m, 1H), 1.15 (d, J=6.4 Hz, 2H), 1.00 (d, J=6.4 Hz, 1H), 0.90 (t, J=7.3 Hz, 3H).

Example 426 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-1-(trifluoromethyl)propyl]amino]-3-pyridyl]-N-(1,1-dioxothian-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 159) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid. MS (ESI): mass calcd. for C₂₅H₂₈F₇N₅O₄S₂, 659.6; m/z found, 659.9 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.99-8.92 (m, 1H), 8.01 (s, 1H), 7.71-7.63 (m, 1H), 7.06-6.72 (m, 2H), 4.87-4.63 (m, 1H), 4.31-4.03 (m, 3H), 3.96-3.72 (m, 1H), 3.10-2.98 (m, 2H), 2.60-2.49 (m, 2H), 2.26-2.12 (m, 3H), 2.11-1.99 (m, 3H), 1.84-1.69 (m, 1H), 1.64-1.50 (m, 1H), 1.15 (d, J=6.4 Hz, 2H), 1.00 (d, J=6.4 Hz, 1H), 0.90 (t, J=7.3 Hz, 3H).

Example 427 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-(tert-butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1R)-2-hydroxy-1-methyl-ethyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 4-((s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 154) for ethyl 4-((1R,4R)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₃₁F₂N₅O₃S, 507.6; m/z found, 508.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.46 (d, J=8.6 Hz, 1H), 7.95 (s, 1H), 7.09-6.76 (m, 3H), 4.83-4.77 (m, 1H), 4.49-4.38 (m, 1H), 4.04-3.89 (m, 2H), 3.50-3.35 (m, 2H), 1.50-1.24 (m, 15H), 1.20-1.07 (m, 5H).

Example 428 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-4-[(2S)-4,4-difluoro-2-methyl-pyrrolidine-1-carbonyl]-N-[(1R)-2-hydroxy-1-methyl-ethyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 110) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₉F₄N₅O₃S, 531.6; m/z found, 532.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.57-8.47 (m, 1H), 7.99 (s, 1H), 7.11-6.73 (m, 3H), 4.90-4.82 (m, 1H), 4.62-4.26 (m, 1H), 4.09-3.78 (m, 3H), 3.54-3.40 (m, 2H), 2.66-2.55 (m, 1H), 2.30-2.06 (m, 1H), 1.40 (s, 9H), 1.21 (d, J=6.5 Hz, 2H), 1.17 (d, J=7.0 Hz, 3H), 1.06 (d, J=6.5 Hz, 1H).

Example 429 5-(6-(tert-Butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-((1r,3S)-3-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (1R,3R)-3-aminocyclobutan-1-ol for (R)-(−)-2-amino-1-propanol and ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 110) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₉F₄N₅O₃S, 543.6; m/z found, 544.0 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.01-7.94 (m, 1H), 7.23-7.17 (m, 1H), 6.90-6.46 (m, 2H), 4.85 (s, 1H), 4.72-4.55 (m, 2H), 4.55-4.45 (m, 1H), 4.11-3.72 (m, 2H), 2.62-2.36 (m, 5H), 2.18-1.98 (m, 1H), 1.87 (s, 1H), 1.44 (s, 9H), 1.34 (d, J=6.0 Hz, 2H), 1.15 (d, J=6.4 Hz, 1H).

Example 430 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-(tert-butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1R,3R)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 161) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1R,3R)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₃S, 533.6; m/z found, 534.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.82 (d, J=8.4 Hz, 1H), 7.94 (s, 1H), 7.11-6.74 (m, 3H), 4.53-4.37 (m, 3H), 4.21-4.13 (m, 1H), 3.95-3.86 (m, 1H), 2.05-1.85 (m, 2H), 1.83-1.69 (m, 2H), 1.62-1.49 (m, 1H), 1.49-1.23 (m, 16H), 1.21-1.06 (m, 2H).

Example 431 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-4-[(2S)-4,4-difluoro-2-methyl-pyrrolidine-1-carbonyl]-N-(1,1-dioxothian-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 162) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and. MS (ESI): mass calcd. for C₂₅H₃₁F₄N₅O₄S₂, 605.7; m/z found, 606.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.04-8.97 (m, 1H), 7.99 (s, 1H), 7.11-6.72 (m, 3H), 4.72-4.17 (m, 2H), 4.16-4.01 (m, 1H), 4.00-3.79 (m, 1H), 3.43-3.37 (m, 2H), 3.16-3.04 (m, 2H), 2.66-2.55 (m, 1H), 2.31-2.03 (m, 5H), 1.40 (s, 9H), 1.22 (d, J=6.0 Hz, 2H), 1.04 (d, J=6.5 Hz, 1H).

Example 432 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1R,3R)-3-hydroxycyclopentyl]-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 163) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1R,3R)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₃S, 521.6; m/z found, 522.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.80 (d, J=8.4 Hz, 1H), 7.95 (s, 1H), 7.11-6.73 (m, 3H), 4.52-4.48 (m, 1H), 4.47-4.37 (m, 1H), 4.22-4.09 (m, 1H), 4.03-3.92 (m, 1H), 3.27-3.23 (m, 1H), 2.05-1.86 (m, 3H), 1.85-1.68 (m, 4H), 1.66-1.49 (m, 2H), 1.48-1.40 (m, 2H), 1.36 (s, 9H), 1.05 (d, J=6.2 Hz, 2H), 0.83 (d, J=6.4 Hz, 1H).

Example 433 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-(tert-butylamino)-4-(difluoromethyl)-3-pyridyl]-N-(1,1-dioxothian-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 161) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₄S₂, 581.7; m/z found, 582.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.05 (d, J=8.4 Hz, 1H), 7.94 (s, 1H), 7.09-6.78 (m, 3H), 4.48-4.41 (m, 1H), 4.24-4.12 (m, 1H), 3.98-3.92 (m, 1H), 3.10-3.01 (m, 2H), 2.27-2.13 (m, 2H), 2.08-1.99 (m, 2H), 1.52-1.24 (m, 17H), 1.22-1.09 (m, 2H).

Example 434 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-(tert-butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1R,2R)-2-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 161) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1R,2R)-2-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₃S, 533.6; m/z found, 534.0 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.07 (s, 1H), 7.35-7.31 (m, 1H), 6.89-6.60 (m, 2H), 4.86 (s, 1H), 4.70 (s, 1H), 4.20-4.14 (m, 1H), 4.08-3.99 (m, 2H), 2.33-2.22 (m, 1H), 2.16-2.05 (m, 1H), 1.94-1.57 (m, 8H), 1.50-1.24 (m, 14H).

Example 435 5-[6-(tert-Butylamino)-4-(difluoromethyl)-3-pyridyl]-N-(1,1-dioxothian-4-yl)-4-[(2S)-2-methylpyrrolidine-1-carbonyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 163) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid. MS (ESI): mass calcd. for C₂₅H₃₃F₂N₅O₄S₂, 569.7; m/z found, 570.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.08-9.02 (m, 1H), 7.98 (s, 1H), 7.13-6.77 (m, 3H), 4.28-4.15 (m, 1H), 4.07-3.97 (m, 1H), 3.33-3.29 (m, 3H), 3.14-3.03 (m, 2H), 2.30-2.15 (m, 2H), 2.13-2.02 (m, 2H), 2.00-1.72 (m, 3H), 1.71-1.52 (m, 1H), 1.50-1.43 (m, 1H), 1.39 (s, 9H), 1.08 (d, J=6.4 Hz, 2H), 0.87 (d, J=6.4 Hz, 1H).

Example 436 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-[[(1S)-1-cyclopropyl-2,2,2-trifluoro-ethyl]amino]-4-(difluoromethyl)-3-pyridyl]-N-(1,1-dioxothian-4-yl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 164) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid. MS (ESI): mass calcd. for C₂₇H₃₀F₅N₅O₄S₂, 647.7; m/z found, 648.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.10 (d, J=8.4 Hz, 1H), 8.02 (s, 1H), 7.89 (d, J=9.3 Hz, 1H), 7.16-6.87 (m, 2H), 4.56-4.42 (m, 2H), 4.28-4.16 (m, 1H), 4.06-4.00 (m, 1H), 3.41-3.36 (m, 1H), 3.14-3.04 (m, 2H), 2.30-2.17 (m, 2H), 2.11-2.03 (m, 2H), 1.53-1.28 (m, 7H), 1.27-1.08 (m, 3H), 0.69-0.59 (m, 1H), 0.57-0.44 (m, 2H), 0.36-0.24 (m, 1H).

Example 437 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-[[(1S)-1-cyclopropyl-2,2,2-trifluoro-ethyl]amino]-4-(difluoromethyl)-3-pyridyl]-N-[(1R,3R)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 165) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1R,3R)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₇H₃₀F₅N₅O₃S, 599.6; m/z found, 600.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.87 (d, J=8.2 Hz, 1H), 8.02 (s, 1H), 7.89 (d, J=9.3 Hz, 1H), 7.16-6.86 (m, 2H), 4.57-4.40 (m, 4H), 4.24-4.16 (m, 1H), 4.02-3.95 (m, 1H), 2.09-1.88 (m, 2H), 1.86-1.73 (m, 2H), 1.65-1.52 (m, 1H), 1.51-1.27 (m, 7H), 1.26-1.09 (m, 3H), 0.69-0.58 (m, 1H), 0.57-0.44 (m, 2H), 0.35-0.26 (m, 1H).

Example 438 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1R,3R)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 153) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1R,3R)-2-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₅H₂₈F₅N₅O₃S, 573.6; m/z found, 574.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.82 (d, J=7.9 Hz, 1H), 8.03 (s, 1H), 7.78 (d, J=8.4 Hz, 1H), 7.13-6.80 (m, 2H), 5.08-4.93 (m, 1H), 4.56-4.37 (m, 3H), 4.18 (s, 1H), 4.00 (s, 1H), 2.04-1.85 (m, 2H), 1.83-1.71 (m, 2H), 1.60-1.12 (m, 13H).

Example 439 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-[[(1S)-1-cyclopropyl-2,2,2-trifluoro-ethyl]amino]-4-(difluoromethyl)-3-pyridyl]-N-[(1R,2R)-2-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 165) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1R,2R)-2-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₇H₃₀F₅N₅O₃S, 599.6; m/z found, 600.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.78 (d, J=8.2 Hz, 1H), 8.03 (s, 1H), 7.89 (d, J=9.3 Hz, 1H), 7.17-6.87 (m, 2H), 4.83 (d, J=5.1 Hz, 1H), 4.57-4.42 (m, 2H), 4.10-3.95 (m, 3H), 2.00-1.80 (m, 2H), 1.69-1.53 (m, 3H), 1.52-1.28 (m, 7H), 1.27-1.07 (m, 3H), 0.69-0.58 (m, 1H), 0.57-0.44 (m, 2H), 0.37-0.26 (m, 1H).

Example 440 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-(tert-butylamino)-4-(difluoromethyl)-3-pyridyl]-N-[(1S,2S)-2-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 155) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,2S)-2-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₆H₃₃F₂N₅O₃S, 533.6; m/z found, 534.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.72 (d, J=8.2 Hz, 1H), 7.95 (s, 1H), 7.09-6.77 (m, 3H), 4.79 (d, J=4.9 Hz, 1H), 4.47-4.41 (m, 1H), 4.06-3.89 (m, 3H), 1.97-1.77 (m, 2H), 1.66-1.50 (m, 3H), 1.47-1.23 (m, 16H), 1.21-1.07 (m, 2H).

Example 441 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-[[(1S)-1-cyclopropyl-2,2,2-trifluoro-ethyl]amino]-4-(difluoromethyl)-3-pyridyl]-N-[(1S,3S)-3-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 165) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,3S)-3-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₇H₃₀F₅N₅O₃S, 599.6; m/z found, 600.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.88 (d, J=8.4 Hz, 1H), 8.02 (s, 1H), 7.90 (d, J=9.0 Hz, 1H), 7.16-6.87 (m, 2H), 4.56-4.42 (m, 4H), 4.24-4.17 (m, 1H), 4.02-3.95 (m, 1H), 2.08-1.89 (m, 2H), 1.86-1.74 (m, 2H), 1.64-1.53 (m, 1H), 1.52-1.27 (m, 7H), 1.26-1.09 (m, 3H), 0.69-0.60 (m, 1H), 0.56-0.44 (m, 2H), 0.35-0.25 (m, 1H).

Example 442 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-[[(1S)-1-cyclopropyl-2,2,2-trifluoro-ethyl]amino]-4-(difluoromethyl)-3-pyridyl]-N-[(3R,4S)-4-hydroxytetrahydrofuran-3-yl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 165) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (3S,4R)-4-aminotetrahydrofuran-3-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₆H₂₈F₅N₅O₄S, 601.6; m/z found, 602.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.06-8.98 (m, 1H), 8.03 (s, 1H), 7.90 (d, J=9.3 Hz, 1H), 7.17-6.87 (m, 2H), 5.33 (d, J=4.0 Hz, 1H), 4.58-4.42 (m, 2H), 4.36-4.31 (m, 1H), 4.21 (br s, 1H), 4.03-3.96 (m, 2H), 3.95-3.90 (m, 1H), 3.69-3.63 (m, 1H), 3.55-3.48 (m, 1H), 1.50-1.27 (m, 6H), 1.26-1.09 (m, 3H), 0.70-0.59 (m, 1H), 0.56-0.44 (m, 2H), 0.36-0.25 (m, 1H).

Example 443 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-((1R*,2R*)-2-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 165) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and trans-2-aminocyclobutan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride followed by SFC purification (Stationary phase: AY, 250×30 mm, 10 m, (eluent:30% (v/v) supercritical CO₂ in EtOH and H₂O with 0.1% NH₃). MS (ESI): mass calcd. for C₂₆H₂₈F₅N₅O₃S, 585.6; m/z found, 586.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.12 (d, J=7.7 Hz, 1H), 7.98 (s, 1H), 7.89 (d, J=9.0 Hz, 1H), 7.10-6.81 (m, 2H), 5.39 (d, J=6.8 Hz, 1H), 4.51-4.38 (m, 2H), 4.16-4.04 (m, 2H), 3.98-3.89 (m, 1H), 1.95-1.78 (m, 2H), 1.51-1.25 (m, 8H), 1.24-1.06 (m, 3H), 0.64-0.56 (m, 1H), 0.52-0.39 (m, 2H), 0.30-0.22 (m, 1H).

Example 444 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)-N-((1S*,2S*)-2-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 165) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and trans-2-aminocyclobutan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride followed by SFC purification (Stationary phase: AY, 250×30 mm, 10 μm (eluent: 30% (v/v) supercritical CO₂ in EtOH and H₂O with 0.1% NH₃). MS (ESI): mass calcd. for C₂₆H₂₈F₅N₅O₃S, 585.6; m/z found, 586.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.17-9.10 (m, 1H), 8.00 (s, 1H), 7.87 (d, J=9.3 Hz, 1H), 7.13-6.84 (m, 2H), 5.31-5.26 (m, 1H), 4.55-4.39 (m, 2H), 4.17-4.06 (m, 2H), 4.00-3.93 (m, 1H), 1.96-1.87 (m, 1H), 1.87-1.78 (m, 1H), 1.54-1.25 (m, 8H), 1.25-1.06 (m, 3H), 0.66-0.57 (m, 1H), 0.53-0.41 (m, 2H), 0.32-0.23 (m, 1H).

Example 445 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1R)-2-hydroxy-1,2-dimethyl-propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 59) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (R)-4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide (Intermediate 166) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅₃S, 575.6; m/z found, 576.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.10-8.03 (m, 2H), 7.79 (d, J=8.8 Hz, 1H), 7.12-6.84 (m, 2H), 5.09-4.95 (m, 1H), 4.74 (s, 1H), 4.48-4.39 (m, 1H), 4.15-4.06 (m, 1H), 3.93-3.84 (m, 1H), 1.62-1.17 (m, 12H), 1.16-1.06 (m, 8H).

Example 446 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1S)-2-hydroxy-1,2-dimethyl-propyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 3 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) for 5-bromo-N-cyclohexyl-4-(trifluoromethyl)pyridin-2-amine and (S)-4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(3-hydroxy-3-methylbutan-2-yl)thiazole-2-carboxamide (Intermediate 167) for 4-(4-fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)thiazole-2-carboxamide. MS (ESI): mass calcd. for C₂₅H₃₀F₅N₅O₃S, 575.6; m/z found, 576.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.11-8.00 (m, 2H), 7.78 (d, J=9.0 Hz, 1H), 7.14-6.81 (m, 2H), 5.10-4.94 (m, 1H), 4.73 (s, 1H), 4.49-4.39 (m, 1H), 4.16-4.08 (m, 1H), 3.88 (s, 1H), 1.53-1.28 (m, 11H), 1.19-1.04 (m, 9H).

Example 447 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-[(1R)-2-hydroxy-1-methyl-ethyl]thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxylate (Intermediate 96) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyrid6517in-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₂H₂₄F₇N₅O₃S, 571.5; m/z found, 571.9 [M+H]⁺. ¹HNMR (400 MHz, DMSO-d₆) δ 8.54-8.43 (m, 1H), 8.05 (s, 1H), 7.78-7.70 (m, 1H), 7.08-6.74 (m, 2H), 5.07-4.93 (m, 1H), 4.85-4.55 (m, 1H), 4.35-4.21 (m, 1H), 4.18-3.74 (m, 3H), 3.51-3.36 (m, 2H), 2.62-2.53 (m, 1H), 2.23-2.03 (m, 1H), 1.31 (d, J=6.8 Hz, 3H), 1.20-1.12 (m, 5H), 1.05 (d, J=6.2 Hz, 1H).

Example 448 4-[(2S)-4,4-Difluoro-2-methyl-pyrrolidine-1-carbonyl]-5-[4-(difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-N-tetrahydropyran-4-yl-thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting tetrahydro-2H-pyran-4-amine for (R)-(−)-2-amino-1-propanol and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridine-3-yl)thiazole-2-carboxylate (Intermediate 96) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₆F₇N₅O₃S, 597.6; m/z found, 598.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.86-8.80 (m, 1H), 8.05 (s, 1H), 7.78-7.71 (m, 1H), 7.10-6.73 (m, 2H), 5.06-4.58 (m, 1H), 4.33-4.20 (m, 1H), 4.17-3.76 (m, 5H), 3.40-3.34 (m, 2H), 2.62-2.53 (m, 1H), 2.26-2.02 (m, 1H), 1.79-1.63 (m, 4H), 1.31 (d, J=6.8 Hz, 3H), 1.18 (d, J=6.4 Hz, 2H), 1.02 (d, J=6.2 Hz, 1H).

Example 449 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-((1R,3S)-3-hydroxycyclobutyl)thiazole-2-carboxamide

The title compound was prepared as described in Example 148 substituting (1R,3R)-3-aminocyclobutan-1-ol for (R)-(−)-2-amino-1-propanol and ethyl 4-((S)-4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 158) for ethyl (S)-5-(6-(tert-butylamino)-4-(difluoromethyl)pyridin-3-yl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₄H₂₆F₇N₅O₃S, 597.6; m/z found, 597.9 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 9.19-9.10 (m, 1H), 8.07 (s, 1H), 7.76-7.67 (m, 1H), 7.13-6.77 (m, 2H), 5.06 (d, J=5.0 Hz, 1H), 4.94-4.65 (m, 1H), 4.55-4.44 (m, 1H), 4.38-4.26 (m, 2H), 4.20-4.08 (m, 1H), 4.01-3.85 (m, 1H), 2.65-2.57 (m, 1H), 2.46-2.38 (m, 2H), 2.22-2.08 (m, 3H), 1.90-1.79 (m, 1H), 1.68-1.55 (m, 1H), 1.24-1.03 (m, 3H), 0.96 (d, J=7.3 Hz, 3H).

Example 450 5-[4-(Difluoromethyl)-6-[[(1S)-2,2,2-trifluoro-1-methyl-ethyl]amino]-3-pyridyl]-2-(3-methylsulfonylazetidine-1-carbonyl)thiazol-4-yl]-[(2S)-2-methylpyrrolidin-1-yl]methanone

The title compound was prepared as described in Example 393 substituting ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate (Intermediate 94) for ethyl 5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxylate. MS (ESI): mass calcd. for C₂₃H₂₆F₅N₅O₄S₂, 595.1; m/z found, 595.8 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.09-8.01 (m, 1H), 6.75-6.69 (m, 1H), 6.76-6.65 (m, 1H), 5.11-4.94 (m, 3H), 4.60-4.50 (m, 2H), 4.22-4.10 (m, 2H), 3.67-3.41 (m, 2H), 3.07-2.95 (m, 3H), 2.12-2.03 (m, 1H), 2.01-1.85 (m, 1H), 1.83-1.74 (m, 1H), 1.60-1.51 (m, 1H), 1.41 (d, J=6.8 Hz, 3H), 1.29-1.20 (m, 2H), 1.09-0.96 (m, 1H).

Example 451 4-(7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-[6-[[(1S)-1-cyclopropyl-2,2,2-trifluoro-ethyl]amino]-4-(difluoromethyl)-3-pyridyl]-N-[(1S,2S)-2-hydroxycyclopentyl]thiazole-2-carboxamide

The title compound was prepared as described in Intermediate 72: Step B, substituting potassium 4-((1R,4R)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(((S)-1-cyclopropyl-2,2,2-trifluoroethyl)amino)-4-(difluoromethyl)pyridin-3-yl)thiazole-2-carboxylate (Intermediate 165) for 4-(tert-butoxycarbonyl)thiazole-2-carboxylic acid and (1S,2S)-2-aminocyclopentan-1-ol for 4-aminotetrahydro-2H-thiopyran-1,1-dioxide hydrochloride. MS (ESI): mass calcd. for C₂₇H₃₀F₅N₅O₃S, 599.6; m/z found, 600.0 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 8.79 (d, J=8.3 Hz, 1H), 8.03 (s, 1H), 7.90 (d, J=9.0 Hz, 1H), 7.18-6.87 (m, 2H), 4.58-4.43 (m, 2H), 4.11-3.94 (m, 3H), 2.00-1.79 (m, 2H), 1.70-1.53 (m, 3H), 1.50-1.29 (m, 8H), 1.25-1.10 (m, 3H), 0.69-0.59 (m, 1H), 0.57-0.45 (m, 2H), 0.36-0.27 (m, 1H).

The following examples of the invention can be prepared by procedures described.

Example 452 N-(2-Hydroxy-2-(methyl-d₃)propyl-3,3,3-d₃)-4-((S)-2-methylpyrrolidine-1-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound can be prepared as described in Example 77 substituting (S)-5-bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 53) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)—N-(2-hydroxy-2-(methyl-d₃)propyl-3,3,3-d₃)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 77: Step C) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 453 5-(6-(((S)-1-Cyclopropylpropyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-N-((1-hydroxycyclopropyl)methyl)-4-((S)-2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound can be prepared as described in Example 77 substituting 5-bromo-N-(1-cyclopropylpropyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 24) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)—N-((1-hydroxycyclopropyl)methyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 78) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 454 4-((S)-4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(3-hydroxy-3-methylcyclobutyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazole-2-carboxamide

The title compound can be prepared as described in Example 77 substituting (S)-5-bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 44) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(3-hydroxy-3-methylcyclobutyl)thiazole-2-carboxamide (Intermediate 79) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 455 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-N-(1,1-dioxidothietan-3-yl)-5-(6-(neopentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound can be prepared as described in Example 77 substituting 5-bromo-N-neopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 22) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(1,1-dioxidothietan-3-yl)thiazole-2-carboxamide (Intermediate 80) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 456 (S)-4-(4,4-Difluoro-2-methylpyrrolidine-1-carbonyl)-5-(4-(difluoromethyl)-6-(neopentylamino)pyridin-3-yl)-N-(1-hydroxy-2-methylpropan-2-yl)thiazole-2-carboxamide

The title compound can be prepared as described in Example 77 substituting 5-bromo-4-(difluoromethyl)-N-neopentylpyridin-2-amine (Intermediate 23) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridine-2-amine and (S)-4-(4,4-difluoro-2-methylpyrrolidine-1-carbonyl)-N-(1-hydroxy-2-methylpropan-2-yl)thiazole-2-carboxamide (Intermediate 81) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 457

(4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazol-2-yl)(3-hydroxy-3-methylazetidin-1-yl)methanone

The title compound can be prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 60) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)thiazol-2-yl)(3-hydroxy-3-methylazetidin-1-yl)methanone (Intermediate 82) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 458 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(4-(difluoromethyl)-6-(((S)-1,1,1-trifluorobutan-2-yl)amino)pyridin-3-yl)-N-(1-hydroxy-2-methylpropan-2-yl)-N-methylthiazole-2-carboxamide

The title compound can be prepared as described in Example 77 substituting (S)-5-bromo-4-(difluoromethyl)-N-(1,1,1-trifluorobutan-2-yl)pyridin-2-amine (Intermediate 49) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(1-hydroxy-2-methylpropan-2-yl)-N-methylthiazole-2-carboxamide (Intermediate 83) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 459 4-((1s,4s)-7-Azabicyclo[2.2.1]heptane-7-carbonyl)-5-(6-(tert-butylamino)-4-(trifluoromethyl)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-N-methylthiazole-2-carboxamide

The title compound can be prepared as described in Example 77 substituting 5-bromo-N-(tert-butyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 41: Step B) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and 4-((1s,4s)-7-azabicyclo[2.2.1]heptane-7-carbonyl)-N-(2-hydroxy-2-methylpropyl)-N-methylthiazole-2-carboxamide (Intermediate 84) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 460 N-(3-Hydroxy-3-methylbutan-2-yl)-N-methyl-4-((S)-2-methylpiperidine-1-carbonyl)-5-(6-(((S)-1,1,1-trifluorobutan-2-yl)amino)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound can be prepared as described in Example 77 substituting (S)-5-bromo-N-(1,1,1-trifluorobutan-2-yl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 53) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and N-(3-hydroxy-3-methylbutan-2-yl)-N-methyl-4-((S)-2-methylpiperidine-1-carbonyl)thiazole-2-carboxamide (Intermediate 85) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 461 5-(6-(((S)-1-Cyclopropylpropyl)amino)-4-(trifluoromethyl)pyridin-3-yl)-4-((S)-2-methylpiperidine-1-carbonyl)-N-(oxetan-3-yl)thiazole-2-carboxamide

The title compound can be prepared as described in Example 77 substituting 5-bromo-N-(1-cyclopropylpropyl)-4-(trifluoromethyl)pyridin-2-amine (Intermediate 24) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-4-(2-methylpiperidine-1-carbonyl)-N-(oxetan-3-yl)thiazole-2-carboxamide (Intermediate 86) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 462 (2-(2,2-Dioxido-2-thia-6-azaspiro[3.3]heptane-6-carbonyl)-5-(4-(trifluoromethyl)-6-(((S)-1,1,1-trifluoropropan-2-yl)amino)pyridin-3-yl)thiazol-4-yl)((S)-2-methylpiperidin-1-yl)methanone

The title compound can be prepared as described in Example 77 substituting (S)-5-bromo-4-(trifluoromethyl)-N-(1,1,1-trifluoropropan-2-yl)pyridin-2-amine (Intermediate 44) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-(2-(2,2-dioxido-2-thia-6-azaspiro[3.3]heptane-6-carbonyl)thiazol-4-yl)(2-methylpiperidin-1-yl)methanone (Intermediate 87) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

Example 463 (S)-(2-(1,1-Dioxidothiomorpholine-4-carbonyl)-5-(6-(neopentylamino)-4-(trifluoromethyl)pyridin-3-yl)thiazol-4-yl)(2-methylpiperidin-1-yl)methanone

The title compound can be prepared as described in Example 77 substituting 5-bromo-N-neopentyl-4-(trifluoromethyl)pyridin-2-amine (Intermediate 22) for 5-bromo-N-(1-methylcyclobutyl)-4-(trifluoromethyl)pyridin-2-amine and (S)-(2-(1,1-dioxidothiomorpholine-4-carbonyl)thiazol-4-yl)(2-methylpiperidin-1-yl)methanone (Intermediate 88) for (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide.

In Vitro Biological Data ThermoFluor® Assay

ThermoFluor® is a fluorescence based assay that estimates ligand binding affinities by measuring the effect of a ligand on protein thermal stability (Pantoliano, M. W., Petrella, E. C., Kwasnoski, J. D., Lobanov, V. S., Myslik, J., Graf, E., Carver, T., Asel, E., Springer, B. A., Lane, P., and Salemme, F. R. (2001) High-density miniaturized thermal shift assays as a general strategy for drug discovery. J Biomol Screen 6, 429-40, and Matulis, D., Kranz, J. K., Salemme, F. R., and Todd, M. J. (2005) Thermodynamic stability of carbonic anhydrase: measurements of binding affinity and stoichiometry using ThermoFluor. Biochemistry 44, 5258-66). This approach is applicable to a wide variety of systems, and rigorous in theoretical interpretation through quantitation of equilibrium binding constants (K_(D)).

In a ThermoFluor® experiment where protein stability is monitored as the temperature is steadily increased, an equilibrium binding ligand causes the midpoint of an unfolding transition (T_(m)) to occur at a higher temperature. The shift in the melting point described as a ΔT_(m) is proportional to the concentration and affinity of the ligand. The compound potency may be compared as a rank order of either ΔT_(m) values at a single compound concentration or in terms of K_(D) values, estimated from concentration response curves.

RORγt ThermoFluor® Assay Construct

For the RORγt construct used in the ThermoFluor® assay, numbering for the nucleotide sequences was based on the reference sequence for human RORγt, transcript variant 2, NCBI Accession: NM_001001523.1 (SEQ ID NO:1). Nucleotides 850-1635 (SEQ ID NO:2) coding for the wild type human RORγt ligand binding domain (RORγt LBD) were cloned into the pHIS1 vector, a modified pET E. coli expression vector (Accelagen, San Diego), containing an in-frame N-terminal His-tag and a TurboTEV protease cleavage site (ENLYFQG, SEQ ID NO:3) upstream of the cloned insert sequence. The amino acid sequence for the RORγt construct used in the Thermofluor® assay is shown as SEQ ID NO:4.

ThermoFluor® experiments were carried out using instruments owned by Janssen Research and Discovery, L.L.C. through its acquisition of 3-Dimensional Pharmaceuticals, Inc. 1,8-ANS (Invitrogen) was used as a fluorescent dye. Protein and compound solutions are dispensed into black 384-well polypropylene PCR microplates (Abgene) and overlayed with silicone oil (1 μL, Fluka, type DC 200) to prevent evaporation.

Bar-coded assay plates are robotically loaded onto a thermostatically controlled PCR-type thermal block and then heated at a typical ramp-rate of 1° C./min for all experiments. Fluorescence was measured by continuous illumination with UV light (Hamamatsu LC6) supplied via fiber optic and filtered through a band-pass filter (380-400 nm; >6 OD cutoff). Fluorescence emission of the entire 384-well plate was detected by measuring light intensity using a CCD camera (Sensys, Roper Scientific) filtered to detect 500±25 nm, resulting in simultaneous and independent readings of all 384 wells. Images were collected at each temperature, and the sum of the pixel intensity in a given area of the assay plate was recorded versus temperature. Reference wells contained RORγt without compounds, and the assay conditions were as follows:

-   -   0.065 mg/mL RORγt     -   60 μM 1,8-ANS     -   100 mM Hepes, pH 7.0     -   10 mM NaCl     -   2.5 mM GSH     -   0.002% Tween-20

Project compounds were arranged in a pre-dosed mother plate (Greiner Bio-one) wherein compounds are serially diluted in 100% DMSO by 1:2 from a high concentration of 10 mM over 12 columns within a series (column 12 is a reference well containing DMSO, no compound). The compounds were robotically dispensed directly into assay plates (1×=46 nL) using a Hummingbird capillary liquid handling instrument (Digilab). Following compound dispense, protein and dye in buffer was added to achieve the final assay volume of 3 μL, followed by 1 μL of silicone oil.

The binding affinity was estimated as described previously (Matulis, D., Kranz, J. K., Salemme, F. R., and Todd, M. J. (2005) Thermodynamic stability of carbonic anhydrase: measurements of binding affinity and stoichiometry using ThermoFluor®. Biochemistry 44, 5258-66) using the following thermodynamic parameters of protein unfolding:

Reference RORγt T_(m): 47.8° C.

ΔH_((Tm))=115 kcal/mol

ΔC_(p(Tm))=3 kcal/mol

Cell Based Biological Data RORγt (Full-Length Human) Reporter Assay:

Three similar reporter assay protocols, shown below, have been used to test the functional activity of RORγt modulatory compounds on transcriptional activation driven by full-length human RORγt. All three provide similar data and can be used interchangeably.

Conditions A

Cells used in this assay were transiently co-transfected with three different plasmids, one expressing the GAL4-DNA binding domain (DBD)-RORγt fusion protein under control of a CMV promoter (NH₂-Gal4-DBD:RORC—COOH in pCMV-BD, Stratagene #211342), and two reporter plasmids—the firefly luciferase reporter under control of a GAL4 promoter (pFR-Luc 2×GAL4) and Renilla luciferase reporter under control of CMV promoter (pRL-CMV, Promega #E2261).

The full-length coding sequence was used for human RORγt, i.e., nucleotides 142-1635 of human RORγt, transcript variant 2, NCBI Accession: NM_001001523.1 (SEQ ID NO:1). HEK293T cells were plated at 35000 per well in 96-well plate in medium of MEM with 8.6% FBS. After 18-22 hours incubation, the transfection was carried out by using a PEI solution with 170.5 ng total DNA/well (50 ng pCMV-BD-ROR plus 20 ng of pFR-Luc reporter and 0.5 ng of pRL-CMV reporter plus 100 ng Carrier DNA (Clontech #630440) for each well). 4-6 hours after transfection, cells were treated with compounds for overnight in the medium with final concentration of FBS 1.1% and DMSO 0.1%. After overnight (16 to 20 hours) incubation, media were removed and cells were lysed with 20 μL 1× Passive Lysis Buffer (Promega) for 10-15 minutes. Luminescence was measured using a BMG LUMIstar OPTIMA plate reader, after addition of 75 μL/well firefly luciferase buffer, followed by 75 L/well Renilla luciferase buffer. To calculate the effect of compounds on RORγt activity, firefly values were normalized against values of DMSO only and values of reference compound at saturating concentration, then further normalized against Renilla signals. IC50s were generated by plotting final Renilla normalized data against compound concentration and percent inhibition was calculated against DMSO control.

Conditions B

Cells used in this assay were transiently co-transfected with three different plasmids, one expressing the GAL4-DNA binding domain (DBD)-RORγt fusion protein under control of a CMV promoter (NH₂-Gal4-DBD:RORC—COOH in pCMV-BD, Stratagene #211342), and two reporter plasmids—the firefly luciferase reporter under control of a GAL4 promoter (pFR-Luc 2×GAL4) and Renilla luciferase reporter under control of CMV promoter (pRL-CMV, Promega #E2261). The full-length coding sequence was used for human RORγt, i.e., nucleotides 142-1635 of human RORγt, transcript variant 2, NCBI Accession: NM_001001523.1 (SEQ ID NO:1). HEK293T cells were plated at 35,000 per well in 96-well plate in medium of DMEM with 10% FBS. After 18-22 hours incubation, the transfection was carried out by using a PEI solution with 170.5 ng total DNA/well (50 ng pCMV-BD-ROR plus 20 ng of pFR-Luc reporter and 0.5 ng of pRL-CMV reporter plus 100 ng Carrier DNA (Clontech #630440) for each well). 4-6 hours after transfection, cells were treated with compounds for overnight in the medium with final concentration of FBS 1.3% and DMSO 0.1%. After overnight (16 to 20 hours) incubation, media were removed and cells were lysed with 50 μL Glo Lysis Buffer (Promega) for 10-15 minutes followed by 10 minute incubation with 50 μL Dual Glo reagent (Promega) at room temperature. Firefly luciferase luminescence was measured using a BMG Pherastar plate reader. To each well, 50 μL Stop and Glo reagent was added and incubated for 10 minutes at room temperature. Renilla luminescence was measured using a BMG Pherastar plate reader. To calculate the effect of compounds on RORγt activity, firefly values were normalized against values of DMSO only and values of reference compound at saturating concentration, then further normalized against Renilla signals. IC50s were generated by plotting final Renilla normalized data against compound concentration and percent inhibition was calculated against DMSO control.

Conditions C

Cells used in this assay were transiently co-transfected with three different plasmids, one expressing the GAL4-DNA binding domain (DBD)-RORγt fusion protein under control of a CMV promoter (NH₂-Gal4-DBD:RORC—COOH in pCMV-BD, Stratagene #211342), and two reporter plasmids—the firefly luciferase reporter under control of a GAL4 promoter (pFR-Luc 2×GAL4) and Renilla luciferase reporter under control of CMV promoter (pRL-CMV, Promega #E2261). The full-length coding sequence was used for human RORγt, i.e., nucleotides 142-1635 of human RORγt, transcript variant 2, NCBI Accession: NM_001001523.1 (SEQ ID NO:1). HEK293T cells were plated at 8750 cells per well in 384-well plate in medium of DMEM with 10% FBS. After 18-22 hours incubation, the transfection was carried out by using a PEI solution with 42.6 ng total DNA/well (12.5 ng pCMV-BD-ROR plus 5 ng of pFR-Luc reporter and 0.125 ng of pRL-CMV reporter plus 25 ng Carrier DNA (Clontech #630440) for each well). 4-6 hours after transfection, cells were treated with compounds for overnight in the medium with final concentration of FBS 1.3% and DMSO 0.1%. After overnight (16 to 20 hours) incubation, media were removed and cells were lysed with 20 μL Glo Lysis Buffer (Promega) for 10-15 minutes followed by 10 minute incubation with 20 μL Dual Glo reagent (Promega) at room temperature. Firefly luciferase luminescence was measured using a BMG Pherastar plate reader. To each well, 20 μL Stop and Glo reagent was added and incubated for 10 minutes at room temperature. Renilla luminescence was measured using a BMG Pherastar plate reader. To calculate the effect of compounds on RORγt activity, firefly values were normalized against values of DMSO only and values of reference compound at saturating concentration, then further normalized against Renilla signals. IC50s were generated by plotting final Renilla normalized data against compound concentration and percent inhibition was calculated against DMSO control.

Human Th17 Assay

The human Th17 assay tests the effect of RORγt modulatory compounds on IL-17 production by CD4 T cells under conditions which favor Th17 differentiation. Total CD4+ T cells were isolated from the peripheral blood mononuclear cells (PBMC) of healthy donors using a CD4+ T cell isolation kit II, following the manufacturer's instructions (Miltenyi Biotec). Cells were resuspended in a medium of RPMI-1640 supplemented with 10% fetal bovine serum, penicillin, streptomycin, glutamate, and β-mercaptoethanol and were added to 96-well plates at 1.5×105 per 100 μL per well. 50 μL of compound at titrated concentrations in DMSO were added into each well at final DMSO concentration at 0.2%. Cells were incubated for 1 hour, then 50 μL of Th17 cell differentiation medium was added to each well. The final concentrations of antibodies and cytokines (R&D Systems) in differentiation medium were: 3×10⁶/mL anti-CD3/CD28 beads (prepared using human T cell activation/expansion kit, Miltenyi Biotec), 10 μg/mL anti-IL4, 10 μg/mL anti-IFNγ, 10 ng/mL IL10, 10 ng/mL IL23, 50 ng/mL IL6, 3 ng/mL TGFβ and 20 U/mL IL2. Cells were cultured at 37° C. and 5% CO₂ for 3 days. Supernatants were collected and the accumulated IL-17 in culture was measured by using MULTI-SPOT® Cytokine Plate following manufacture's instruction (Meso Scale Discovery). The plate was read using Sector Imager 6000, and IL-17 concentration was extrapolated from the standard curve. The IC50s were determined by GraphPad.

TABLE 1 RORγt RORγt (FL) RORγt (FL) Human (FL) Reporter RORγt (FL) Reporter Th17 Reporter Assay A, % Reporter Assay B or C, Assay, Example ThermoFluor ® Assay A, inhibition @ Assay B or C, % inhibition IC₅₀ # Assay, Kd (μM) IC₅₀ (μM) 6 μM IC₅₀ (μM) @ 6 μM (μM) 1 0.035 0.079  100** ND ND ND 2 0.040 ND ND 0.077  95* ND 3 0.0096 0.035  106** ND ND 0.040 4 0.00098 0.0090 106 ND ND ND 5 0.00025 0.0090 104 ND ND ND 6 −0.010 0.16 110 ND ND ND 7 0.23 0.62  80 ND ND ND 8 0.12 0.34  95 ND ND ND 9 0.077 0.33 104 ND ND ND 10 0.0081 0.071 108 ND ND ND 11 0.0026 0.017  107** ND ND ND 12 0.063 0.85  92 ND ND 0.19 13 0.037 0.10   99** ND ND ND 14 0.033 0.076 105 ND ND ND 15 0.0075 0.039  105** ND ND ND 16 0.13 0.47 105 ND ND ND 17 0.00015 0.0090   95** ND ND ND 18 0.080 0.62 106 ND ND ND 19 0.0044 0.032  99 ND ND 0.040 20 0.052 0.20 110 ND ND ND 21 0.13 0.54 100 ND ND ND 22 0.44 0.91  84 ND ND ND 23 0.030 0.079  96 ND ND ND 24 0.020 0.097 107 ND ND ND 25 0.12 ND ND 0.22   102.03 ND 26 0.0095 ND ND 0.037   110.91 ND 27 0.00052 ND ND 0.0084   106.29 0.016 28 0.00017 ND ND 0.014   123.45 ND 29 0.022 ND ND 0.022   104.84 ND 30 0.0028 ND ND 0.020   103.81 ND 31 0.00015 ND ND 0.0045   110.67 ND 32 0.00026 ND ND 0.0022   108.97 ND 33 0.00043 ND ND 0.0052   108.55 ND 34 0.00029 ND ND 0.0069   105.12 ND 35 0.0039 ND ND 0.020  113.8 ND 36 0.0017 ND ND 0.016   116.32 ND 37 0.00065 ND ND 0.014    92.175 0.052 38 0.0018 ND ND 0.015   108.34 0.081 39 0.00012 ND ND 0.013   104.57 ND 40 0.0028 ND ND 0.013   102.02 0.056 41 0.00074 ND ND 0.0076   103.11 0.043 42 0.0093 ND ND 0.042   110.78 ND 43 0.0049 ND ND 0.022   107.46 ND 44 0.0025 ND ND 0.020   111.26 ND 45 0.00062 ND ND 0.010   110.64 ND 46 0.0042 ND ND 0.029 100* ND 47 0.00050 ND ND 0.0054  96* 0.0098 48 0.011 ND ND 0.023 111* ND 49 0.0033 ND ND 0.0076  99* ND 50 0.071 ND ND 0.058 100* ND 51 0.0032 ND ND 0.0048 101* 0.021 52 0.0012 ND ND 0.0088 106* 0.010 53 0.0058 ND ND 0.023 109* ND 54 0.012 ND ND 0.046 109* ND 55 0.0079 ND ND 0.031  92* ND 56 0.00034 ND ND 0.0036 106* ND 57 0.079 0.078 106 ND ND ND 58 0.17 0.77  93 ND ND ND 59 ND 0.70  88 ND ND ND 60 0.16 0.43    90.333 ND ND ND 61 0.0070 ND ND 0.013 103* ND 62 0.012 0.16  98 ND ND ND 63 ND 0.25  96 ND ND ND 64 0.017 0.063  96 ND ND 0.22 65 ND 0.21 103 ND ND ND 66 0.041 0.15  85 ND ND ND 67 0.052 0.40  98 ND ND ND 68 0.37 1.1  70 ND ND ND 69 0.17 0.63  85 ND ND ND 70 0.036 0.13 108 ND ND ND 71 0.0037 ND ND 0.013 111* ND 72 0.035 ND ND 0.089 104* ND 73 0.011 ND ND 0.074 104* ND 74 0.073 ND ND 0.032 101* ND 75 −0.00023 ND ND 0.0070  108** 0.014 76 −0.00034 ND ND 0.0038   108.44 0.020 77 0.0013 ND ND 0.017 108* ND 78 0.0032 ND ND 0.049 110* 0.014 79 0.0012 ND ND 0.0083 111* ND 80 0.00019 ND ND 0.0047 111* ND 81 0.00017 ND ND 0.0093 105* ND 82 0.0048 ND ND 0.079 117* ND 83 0.00055 ND ND 0.0069  110*** ND 84 0.0012 ND ND 0.018 136* ND 85 0.00053 ND ND 0.027  128*** ND 86 0.00017 ND ND 0.013 127* 0.0028 87 0.0013 ND ND 0.029 140* 0.025 88 0.00019 ND ND 0.010 138* ND 89 0.0052 ND ND 0.024 100* ND 90 0.0014 ND ND 0.11  86* 0.076 91 0.00052 ND ND 0.030  96* 0.019 92 0.0034 ND ND 0.071 106* ND 93 0.0011 ND ND 0.010 121* ND 94 0.00036 ND ND 0.012 115* ND 95 0.00015 ND ND 0.0095 109* ND 96 0.0012 ND ND 0.037 119* ND 97 0.0013 ND ND 0.0036 111* ND 98 0.00041 ND ND 0.0096 110* ND 99 0.00058 ND ND 0.011 108* ND 100 0.00039 ND ND 0.014 108* ND 101 0.0032 ND ND 0.019 107* ND 102 0.00099 ND ND 0.017 116* ND 103 0.00026 ND ND 0.0039 110* ND 104 0.00064 ND ND 0.025 110* ND 105 0.0020 ND ND 0.015 116* ND 106 0.00079 ND ND 0.022 117* ND 107 0.00026 ND ND 0.011 111* ND 108 0.000070 ND ND 0.047 104* ND 109 0.00053 ND ND 0.018 124* ND 110 0.0022 ND ND 0.026 112* ND 111 0.0018 ND ND 0.029 106* 0.017 112 0.00020 ND ND 0.013 110* ND 113 0.0060 ND ND 0.063 110* ND 114 0.00049 ND ND 0.0097 117* ND 115 0.0019 ND ND 0.028 115* 0.022 116 0.0036 ND ND 0.034 110* 0.044 117 0.00078 ND ND 0.0033 107* ND 118 0.00043 ND ND 0.0071   109**** ND 119 0.0015 ND ND 0.017 108* ND 120 0.0017 ND ND 0.026 103* ND 121 0.00065 ND ND 0.025 104* ND 122 0.0017 ND ND 0.033 102* 0.020 123 0.0019 ND ND 0.013 105* ND 124 0.00052 ND ND 0.021 108* 0.0067 125 0.0024 ND ND 0.059 100* ND 126 0.00085 ND ND 0.069  98* ND 127 0.0062 ND ND 0.11 114* ND 128 0.0026 ND ND 0.023 107* 0.018 129 0.0030 ND ND 0.011 104* ND 130 0.0016 ND ND 0.030   98*** ND 131 0.0014 ND ND 0.030 107* ND 132 0.00041 ND ND 0.014 112* ND 133 0.0045 ND ND 0.028 105* ND 134 0.0012 ND ND 0.014 108* ND 135 0.0035 ND ND 0.039 100* 0.044 136 0.016 ND ND 0.79 109* ND 137 0.0011 ND ND 0.012  97* ND 138 0.00062 ND ND 0.012  100*** ND 139 0.0011 ND ND 0.012 107* ND 140 0.0017 ND ND 0.011  89* 0.011 141 0.00068 ND ND 0.023 100* 0.0055 142 0.0014 ND ND 0.027 109* 0.019 143 0.0023 ND ND 0.039 114* ND 144 0.0015 ND ND 0.076 106* 0.013 145 0.0077 ND ND 0.074   76*** ND 146 0.21 ND ND 0.83  98* ND 147 0.0094 ND ND 0.12   94*** ND 148 0.0064 ND ND 0.025  95* ND 149 0.020 ND ND 0.10 108* ND 150 0.0032 ND ND 0.035 111* ND 151 0.00087 ND ND 0.015 104* ND 152 0.00088 ND ND 0.011 101.5 ND 153 0.0011 ND ND 0.052  98* ND 154 0.0010 ND ND 0.098  99* ND 155 0.0011 ND ND 0.0058 103* ND 156 0.0010 ND ND 0.044 102* ND 157 0.032 ND ND 0.19  89* ND 158 0.017 ND ND 0.31  96* ND 159 0.022 ND ND 0.032   93*** ND 160 0.0087 ND ND 0.41 101* ND 161 0.00078 ND ND 0.020 106* ND 162 0.0095 ND ND 0.031 104* ND 163 0.014 ND ND 0.012 114* ND 164 0.0046 ND ND 0.023 105* ND 165 0.0031 ND ND 0.040  98* ND 166 0.0047 ND ND 0.027  94* ND 167 0.0037 ND ND 0.12 100* ND 168 0.0018 ND ND 0.20 106* ND 169 0.0027 ND ND 0.012  94* 0.034 170 0.0019 ND ND 0.024 101* ND 171 0.0040 ND ND 0.016 108* ND 172 0.0012 ND ND 0.039 102* ND 173 0.0058 ND ND 0.055  95* ND 174 0.0014 ND ND 0.025 106* ND 175 0.0058 ND ND 0.044  119*** ND 176 0.0013 ND ND 0.015  115*** ND 177 0.00097 ND ND 0.0066 117* ND 178 0.0020 ND ND 0.0055 102* ND 179 0.0022 ND ND 0.018 105* ND 180 0.0018 ND ND 0.020 113* ND 181 0.0011 ND ND 0.0085 112* ND 182 0.00012 ND ND 0.0081  99* ND 183 0.00022 ND ND 0.034  76* ND 184 0.00070 ND ND 0.049  92* ND 185 0.00023 ND ND 0.015 101* ND 186 0.00018 ND ND 0.016  98* ND 187 0.0068 ND ND 0.14  85* ND 188 0.047 ND ND 0.54  85* ND 189 0.0036 ND ND 0.098 101* ND 190 0.0038 ND ND 0.034 104* ND 191 0.018 ND ND 0.032  98* ND 192 0.0028 ND ND 0.037 101* ND 193 0.0026 ND ND 0.032  82* ND 194 0.0047 ND ND 0.088  85* ND 195 0.00043 ND ND 0.033  85* ND 196 0.00064 ND ND 0.027 109* ND 197 0.0017 ND ND 0.066  91* 0.030 198 0.0025 ND ND 0.053 102* ND 199 0.0054 ND ND 0.12  94* 0.10 200 0.012 ND ND 0.20 104* ND 201 0.00061 ND ND 0.016 102* ND 202 0.0013 ND ND 0.017  98* ND 203 0.0015 ND ND 0.042  97* ND 204 0.0036 ND ND 0.024 105* ND 205 0.0068 ND ND 0.033 103* ND 206 0.0032 ND ND 0.035  106*** ND 207 0.0026 ND ND 0.019  103*** ND 208 0.0044 ND ND 0.054 101* ND 209 0.0034 ND ND 0.046  99* ND 210 0.00069 ND ND 0.021 105* ND 211 0.0082 ND ND 0.014 104* ND 212 0.013 ND ND 0.30 104* ND 213 0.0061 ND ND 0.019 103* ND 214 0.012 ND ND 0.075  98* ND 215 0.012 ND ND 0.10 107* ND 216 0.0041 ND ND 0.0095  96* ND 217 0.0032 ND ND 0.019 109* ND 218 0.0078 ND ND 0.045 111* ND 219 0.0041 ND ND 0.020 112* ND 220 0.0061 ND ND 0.013   111***** ND 221 0.027 ND ND 0.078 103* ND 222 0.010 ND ND 0.012 113* ND 223 0.033 ND ND 0.10 112* ND 224 0.0027 ND ND 0.026 112* ND 225 0.00095 ND ND 0.0068 110* ND 226 0.014 ND ND 0.14  94* ND 227 0.0046 ND ND 0.014  95* ND 228 0.0023 ND ND 0.095   91*** ND 229 0.00097 ND ND 0.042  83* ND 230 0.0024 ND ND 0.015  99* ND 231 0.0014 ND ND 0.058  92* ND 232 0.0034 ND ND 0.069 122* ND 233 0.010 ND ND 0.022 124* ND 234 0.0052 ND ND 0.042 116* ND 235 0.0012 ND ND 0.034 106* ND 236 0.0016 ND ND 0.047 122* ND 237 0.0023 ND ND 0.031 101* ND 238 0.0055 ND ND 0.029  92* ND 239 0.0054 ND ND 0.019 105* ND 240 0.0025 ND ND 0.057 107* ND 241 0.00059 ND ND 0.024 103* ND 242 0.0028 ND ND 0.015  86* ND 243 0.0073 ND ND 0.0068  95* 0.063 244 0.0062 ND ND 0.0083 106* ND 245 0.0016 ND ND 0.026  98* ND 246 0.0013 ND ND 0.011  112*** ND 247 0.00028 ND ND 0.023 100* ND 248 0.0034 ND ND 0.016 102* ND 249 0.0081 ND ND 0.024 103* ND 250 0.0081 ND ND 0.028 106* ND 251 0.021 ND ND 0.072 104* ND 252 0.0012 ND ND 0.035 106* ND 253 0.0019 ND ND 0.0077 108* ND 254 0.00025 ND ND 0.016 107* ND 255 0.016 ND ND 0.16   78*** ND 256 0.0017 ND ND 0.020 123* ND 257 0.0018 ND ND 0.031  98* ND 258 0.0035 ND ND 0.065 110* ND 259 0.0030 ND ND 0.025 101* ND 260 0.0007 ND ND 0.014 112* ND 261 0.0026 ND ND 0.023 104* ND 262 0.0016 ND ND 0.020 104* ND 263 0.0011 ND ND 0.0066 107* ND 264 0.0049 ND ND 0.028 112* ND 265 0.0064 ND ND 0.075  98* ND 266 0.0044 ND ND 0.050 100* ND 267 0.0033 ND ND 0.047 102* ND 268 0.0024 ND ND 0.11 109* ND 269 0.0049 ND ND 0.0082 101* ND 270 0.0035 ND ND 0.0051 102* ND 271 0.0040 ND ND 0.0057 106* ND 272 0.0021 ND ND 0.018 105* ND 273 0.00051 ND ND 0.0052 102* ND 274 0.00097 ND ND 0.036  96* ND 275 0.0020 ND ND 0.014  99* ND 276 0.0061 ND ND 0.016  118*** ND 277 0.0024 ND ND 0.011 113* ND 278 0.0074 ND ND 0.040 100* ND 279 0.018 ND ND 0.062  109*** ND 280 0.0049 ND ND 0.016 110* ND 281 0.21 ND ND 0.83  98* ND 282 0.0014 ND ND 0.019 109* ND 283 0.0019 ND ND 0.054 106* ND 284 0.0081 ND ND 0.11 111* ND 285 0.0029 ND ND 0.064 104* ND 286 0.011 ND ND 0.14 104* ND 287 0.0043 ND ND 0.034 109* ND 288 0.0044 ND ND 0.029 103* ND 289 0.0038 ND ND 0.069  99* ND 290 0.0063 ND ND 0.0065 103* ND 291 0.0069 ND ND 0.12 113* ND 292 0.0061 ND ND 0.040 106* ND 293 0.0020 ND ND 0.013  94* ND 294 0.0013 ND ND 0.013 100* ND 295 0.0029 ND ND 0.014 108* ND 296 0.00050 ND ND 0.0071 108* ND 297 0.018 ND ND 0.050 110* ND 298 0.0034 ND ND 0.0077  99* ND 299 0.00091 ND ND 0.011 103* ND 300 0.0016 ND ND 0.029 100* ND 301 0.030 ND ND 0.084  95* ND 302 0.049 ND ND >3.0  86* ND 303 0.015 ND ND 0.74  88* ND 304 0.0051 ND ND 0.092 102* ND 305 0.0049 ND ND 0.036 100* 0.089 306 0.010 ND ND 0.13 104* ND 307 0.043 ND ND 0.15 102* ND 308 0.096 ND ND 0.26 107* ND 309 0.016 ND ND 0.013  95* ND 310 0.0087 ND ND 0.036  92* ND 311 0.0037 ND ND 0.040 107* ND 312 0.0022 ND ND 0.027 106* ND 313 0.00074 ND ND 0.036 106* ND 314 0.0014 ND ND 0.035 101* ND 315 0.0029 ND ND 0.015   99*** ND 316 0.0029 ND ND 0.032 108* ND 317 0.0024 ND ND 0.014 106* ND 318 0.0081 ND ND 0.028  86* 0.017 319 0.029 ND ND 0.079  91* ND 320 0.0038 ND ND 0.046  98* ND 321 0.0052 ND ND 0.10  87* ND 322 0.0018 ND ND 0.049 106* ND 323 0.0082 ND ND 0.15   97*** ND 324 0.0024 ND ND 0.038  93* ND 325 0.0012 ND ND 0.12  96* ND 326 0.00071 ND ND 0.097  90* ND 327 0.0020 ND ND 0.011  93* ND 328 0.00031 ND ND 0.051  87* ND 329 0.0017 ND ND 0.038  89* ND 330 0.0042 ND ND 0.016  93* ND 331 0.0015 ND ND 0.023  81* ND 332 0.0015 ND ND 0.089 107* ND 333 0.00078 ND ND 0.030  98* ND 334 0.0014 ND ND 0.007 106* ND 335 0.0013 ND ND 0.040 102* ND 336 0.0011 ND ND 0.0056 108* 0.011 337 0.0029 ND ND 0.013 105* ND 338 0.0039 ND ND 0.0077 107* ND 339 0.00097 ND ND 0.0029 109* ND 340 0.0053 ND ND 0.011 111* ND 341 0.0040 ND ND 0.0057 107* ND 342 0.0057 ND ND 0.040 103* ND 343 0.0051 ND ND 0.31  98* ND 344 0.0032 ND ND 0.0053   53**** ND 345 0.016 ND ND 0.063 111* ND 346 0.0014 ND ND 0.013 112* ND 347 0.00038 ND ND 0.0038 124* ND 348 0.00090 ND ND 0.0031 105* ND 349 0.011 ND ND 0.063 105* ND 350 0.0083 ND ND 0.030 110* ND 351 0.00015 ND ND 0.0080    92****** ND 352 0.0011 ND ND 0.042 103* ND 353 0.0016 ND ND 0.020  95* ND 354 0.00097 ND ND 0.015  93* ND 355 0.022 ND ND 0.17  98* ND 356 0.047 ND ND 0.035  94* ND 357 0.0012 ND ND 0.012 106* ND 358 0.0025 ND ND 0.015 119* ND 359 0.0011 ND ND 0.0076 125* ND 360 0.010 ND ND 0.082 106* ND 361 0.00037 ND ND 0.025 105* ND 362 0.0040 ND ND 0.021  99* ND 363 0.013 ND ND 0.13 111* ND 364 0.0079 ND ND 0.039 111* ND 365 0.0081 ND ND 0.052   92*** ND 366 0.010 ND ND 0.063  97* ND 367 0.0021 ND ND 0.021  99* ND 368 0.0017 ND ND 0.0075 110* ND 369 0.00070 ND ND 0.0066 106* ND 370 0.00069 ND ND 0.010  96* ND 371 0.00088 ND ND 0.019 108* ND 372 0.0092 ND ND 0.059 125* ND 373 0.0019 ND ND 0.0046 122* ND 374 0.0016 ND ND 0.0048 121* ND 375 0.0057 ND ND 0.029 105* ND 376 0.0038 ND ND 0.060 101* ND 377 0.0034 ND ND 0.032  91* ND 378 0.018 ND ND 0.079 109* ND 379 0.0024 ND ND 0.055 101* ND 380 0.0016 ND ND 0.018 108* ND 381 0.0067 ND ND 0.012 107* ND 382 0.047 ND ND 0.30 107* ND 383 0.0026 ND ND 0.092 108* ND 384 0.0050 ND ND 0.070  98* ND 385 0.10 ND ND 0.35  95* ND 386 0.0094 ND ND 0.072  99* ND 387 0.0099 ND ND 0.13 102* ND 388 0.0086 ND ND 0.085 103* ND 389 0.0077 ND ND 0.14  90* ND 390 0.012 ND ND 0.028  99* ND 391 0.0042 ND ND 0.035 106* ND 392 0.044 ND ND 0.13 102* ND 393 0.029 ND ND 0.027 118* ND 394 0.0020 ND ND 0.034 114* ND 395 0.040 ND ND 0.034 103* ND 396 0.0011 ND ND 0.021  96* ND 397 0.0012 ND ND 0.0090 118* ND 398 0.0015 ND ND 0.039 109* ND 399 0.0012 ND ND 0.025 100* ND 400 0.013 ND ND 0.056  84* ND 401 0.0043 ND ND 0.038  102*** ND 402 0.0058 ND ND 0.037  99* ND 403 0.0045 ND ND 0.036 108* ND 404 0.0038 ND ND 0.015    98***** ND 405 0.0020 ND ND 0.11  95* ND 406 0.0027 ND ND 0.081    92***** ND 407 0.015 ND ND 0.12 100* ND 408 0.0038 ND ND 0.073  83* ND 409 0.0063 ND ND 0.036 103* ND 410 0.0011 ND ND 0.018  97* ND 411 0.0036 ND ND 0.11 100* ND 412 0.0034 ND ND 0.037 127* ND 413 0.00082 ND ND 0.020  133*** ND 414 0.0017 ND ND 0.013 110* ND 415 0.0011 ND ND 0.064  97* ND 416 0.00043 ND ND 0.037   89*** ND 417 0.0024 ND ND 0.028   94*** ND 418 0.00077 ND ND 0.032 105* ND 419 0.00021 ND ND 0.034  84* ND 420 0.00073 ND ND 0.032 103* ND 421 0.0010 ND ND 0.064   98*** ND 422 0.00062 ND ND 0.023 101* ND 423 0.0011 ND ND 0.038 103* ND 424 0.00023 ND ND 0.063  98* ND 425 0.00018 ND ND 0.050 103* ND 426 0.00037 ND ND 0.079  96* ND 427 0.0030 ND ND 0.0030 113* ND 428 0.0010 ND ND 0.017 113* ND 429 0.0025 ND ND 0.0095   113**** ND 430 0.00060 ND ND 0.013  130*** ND 431 0.00036 ND ND 0.020 107* ND 432 0.0013 ND ND 0.011   122**** ND 433 0.0012 ND ND 0.025 128* ND 434 0.00063 ND ND 0.011 103* ND 435 0.0023 ND ND 0.021 105* ND 436 0.0010 ND ND 0.048  117*** ND 437 0.00044 ND ND 0.016  90* ND 438 0.0040 ND ND 0.083   99*** ND 439 0.00027 ND ND 0.010 102* ND 440 0.00072 ND ND 0.031 104* ND 441 0.00047 ND ND 0.036 106* ND 442 0.0016 ND ND 0.32   96*** ND 443 0.0022 ND ND 0.016 107* ND 444 0.0023 ND ND 0.0045 102* ND 445 0.012 ND ND 0.096  73* ND 446 0.013 ND ND 0.18 108* ND 447 0.0021 ND ND 0.075  89* ND 448 0.00080 ND ND 0.028  99* ND 449 0.0021 ND ND 0.021 108* ND 450 0.050 ND ND 0.23 106* ND 451 0.00029 ND ND 0.29  99* ND ND: value not determined. *% inhibition is shown at 3 μM compound concentration, **% inhibition is shown at 2 μM compound concentration, ***% inhibition is shown at 1 μM compound concentration, ****% inhibition is shown at 0.33 μM compound concentration, *****% inhibition is shown at 0.3 μM compound concentration, ******% inhibition is shown at 0.11 μM compound concentration.

Comparative Data

The 6-amino-pyridin-3-yl thiazole compounds of the present invention demonstrate unexpectedly superior RORγt modulator activity compared to 2-amino-pyridin-3-yl thiazole and 5-amino-pyridin-3-yl thiazole analogs, as shown in Table 2.

TABLE 2 RORγt (FL) Reporter ThermoFluor ® Assay B or Assay, Kd C, IC₅₀ Example # Structure (μM) (μM) Comparator Example 1

3.0 >6 Comparator Example 2

5.8 3 146

0.21 0.83 Table 2 compares the inventive 6-amino-pyridin-3-yl thiazole compound of Example 146 to two analog compounds, Comparator Example 1, which is a 2-amino-pyridin-4-yl thiazole and Comparator Example 2, which is a 5-amino-pyridin-3-yl thiazole. The compound of the invention is surprisingly superior with 7.2 fold improvement in RORγt reporter assay activity compared to Comparator Example 1 and 3.6 fold improvement in RORγt reporter assay activity compared to Comparator Example 2. When comparing the same compounds in the Thermofluor® binding assay, the inventive compound, Example 146, is again surprisingly superior with 14 fold improvement in RORγt Thermofluor® binding assay activity compared to Comparator Example 1 and 27 fold improvement in RORγt Thermofluor® binding assay activity compared to Comparator Example 2.

In addition, the 6-amino-pyridin-3-yl thiazole compounds of the present invention demonstrate unexpectedly superior RORγt modulator activity compared to 6-sulfonamino analogs, as shown in Table 3.

TABLE 3 RORγt (FL) Reporter ThermoFluor ® Assay A, Assay, Kd IC₅₀ Example # Structure (μM) (μM) Comparator Example 3

53 >6 12

0.063 0.85 Thus, the compound of Example 12 demonstrated a desirable IC₅₀ of 0.85 μM. In contrast, the 6-sulfonamino analog demonstrated an IC₅₀ of greater than 6 μM, rendering it unsuitable for development as a therapeutic drug due to undesirable RORγt modulator activity. When comparing the same compounds in the Thermofluor® binding assay, the compound of Example 12 is again surprisingly superior with over 800 fold improvement in RORγt Thermofluor® binding assay activity compared to Comparator Example 3.

Synthesis of Comparator Compound Examples Comparator Intermediate 1 4-Bromo-2-(cyclohexylamino)nicotinonitrile

To a vial was added 2,4-dibromo-nicotinonitrile (300 mg, 1.11 mmol) and cyclohexylamine (0.64 mL, 5.56 mmol) and the resulting mixture was stirred at rt for 5 minutes. The mixture was partitioned between saturated aqueous NaHCO₃ (10 mL), water (10 mL) and EtOAc (20 mL). The aqueous was further extracted with EtOAc (25 mL). The organics were combined, dried over anhydrous Na₂SO₄, filtered and concentrated to dryness. The residue was purified by FCC (EtOAc/hexanes=0/100 to 25/75) to provide the title compound as a white solid.

Comparator Intermediate 2 3-Bromo-5-(cyclohexylamino)isonicotinonitrile

To a vial was added 3,5-dibromo-4-cyanopyridine (500 mg, 1.85 mmol), Pd(OAc)₂ (42 mg, 0.19 mmol), XantPhos (214 mg, 0.37 mmol), Cs₂CO₃ (1.51 g, 4.63 mmol) and cyclohexylamine (0.21 mL, 1.85 mmol). The vial was evacuated and backfilled with nitrogen twice, then 1,4-dioxane (7.1 mL) was added and the resulting mixture was stirred at 80° C. for 4.5 hours. The mixture was allowed to cool to rt, then was partitioned between water (25 mL) and EtOAc (40 mL). The aqueous was further extracted with EtOAc (40 mL), then the organics were combined, dried over anhydrous sodium sulfate, filtered and concentrated to dryness. The residue was purified by FCC (100% DCM) to provide the title compound as a cream-colored solid.

Comparator Intermediate 3 N-(5-Bromo-4-(trifluoromethyl)pyridin-2-yl)propane-2-sulfonamide

To a flask was added 5-bromo-4-(trifluoromethyl)pyridin-2-amine (0.52 g, 2.17 mmol), NaH (60% in mineral oil, 209 mg, 4.3 mmol) and DMF (8.7 mL). The mixture was cooled to 0° C. and stirred at that temperature for 20 minutes. Then, isopropylsulfonyl chloride (310 mg, 2.17 mmol) was added dropwise at 0° C. The mixture was allowed to warm to rt and stirred at that temperature for an additional two hours. The mixture was then poured into ice water (15 mL) and the precipitated solid was collected by filtration to provide the title compound as a yellow solid.

Comparator Example 1 (S)-5-(3-Cyano-2-(cyclohexylamino)pyridin-4-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

An oven-dried vial under nitrogen was charged with (S)—N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide (46 mg, 0.15 mmol, Intermediate 69), 4-bromo-2-(cyclohexylamino)nicotinonitrile (41 mg, 0.15 mmol, Comparator Intermediate 1), K₂CO₃ (81 mg, 0.59 mmol), pivalic acid (6 mg, 0.059 mmol) and butyronitrile (0.91 mL, sparged with nitrogen for 1 hour prior to addition). The mixture was sparged with nitrogen for 30 minutes, then bis(tri-tert-butylphosphine)palladium(0) (7.5 mg, 0.015 mmol) was added and the mixture sparged with nitrogen for 2 minutes. The resulting mixture was stirred for 19 h at 100° C. The reaction mixture was then cooled to room temperature, diluted with water (15 mL), and the aqueous phase was extracted with EtOAc (2×20 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous Na₂SO₄, filtered and concentrated to dryness. The crude product was purified by basic HPLC to provide the title compound as a yellow amorphous solid. MS (ESI): mass calcd. for C₂₆H₃₄N₆O₃S, 510.7; m/z found, 511.1 [M+H]⁺. ¹H NMR (400 MHz, CDCl₃) δ 8.30-8.26 (m, 1H), 7.60-7.51 (m, 1H), 6.69-6.63 (m, 1H), 5.16-5.10 (m, 1H), 4.34-4.25 (m, 1H), 4.06-3.96 (m, 1H), 3.73-3.57 (m, 2H), 3.52-3.45 (m, 2H), 2.20-1.72 (m, 9H), 1.70-1.62 (m, 2H), 1.48-1.38 (m, 2H), 1.35-1.29 (m, 9H), 1.27-1.23 (m, 2H).

Comparator Example 2 (S)-5-(4-Cyano-5-(cyclohexylamino)pyridin-3-yl)-N-(2-hydroxy-2-methylpropyl)-4-(2-methylpyrrolidine-1-carbonyl)thiazole-2-carboxamide

The title compound was prepared as described in Comparator Example 1 using 3-bromo-5-(cyclohexylamino)isonicotinonitrile (Comparator Intermediate 2) in place of 4-bromo-2-(cyclohexylamino)nicotinonitrile. MS (ESI): mass calcd. for C₂₆H₃₄N₆O₃S, 510.7; m/z found, 511.1 [M+H]⁺. ¹H NMR (500 MHz, CDCl₃) δ 8.23 (s, 1H), 8.02-7.96 (m, 1H), 7.59-7.50 (m, 1H), 4.53-4.49 (m, 1H), 4.46-4.25 (m, 1H), 3.78-3.68 (m, 1H), 3.67-3.60 (m, 1H), 3.53-3.45 (m, 3H), 2.19-2.06 (m, 3H), 2.00-1.94 (m, 1H), 1.92 (s, 1H), 1.90-1.79 (m, 3H), 1.71-1.66 (m, 1H), 1.64-1.59 (m, 1H), 1.47-1.37 (m, 2H), 1.33-1.31 (m, 9H), 1.30-1.22 (m, 3H).

Comparator Example 3 4-(4-Fluoropiperidine-1-carbonyl)-N-(2-hydroxy-2-methylpropyl)-5-(6-((1-methylethyl)sulfonamido)-4-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide

The title compound was prepared as described in Example 57 substituting N-(5-bromo-4-(trifluoromethyl)pyridin-2-yl)propane-2-sulfonamide (Comparator Intermediate 3) for 5-bromo-2-(cyclohexylamino)isonicotinonitrile. MS (ESI): mass calcd. for C₂₃H₂₉F₄N₅O₅S₂, 595.2; m/z found, 596.2 [M+H]⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 11.23 (s, 1H), 8.48 (s, 1H), 8.43 (t, J=6.1 Hz, 1H), 7.36 (s, 1H), 4.95-4.83 (m, 1H), 4.70 (s, 1H), 3.95-3.82 (m, 1H), 3.58-3.47 (m, 4H), 3.29 (d, J=6.3 Hz, 2H), 1.95-1.75 (m, 2H), 1.64 (br s, 2H), 1.32 (d, J=6.8 Hz, 6H), 1.13 (s, 6H).

While the foregoing specification teaches the principles of the present invention, with examples provided for the purpose of illustration, it will be understood that the practice of the invention encompasses all of the usual variations, adaptations and/or modifications as come within the scope of the following claims and their equivalents.

All documents cited herein are incorporated by reference. 

We claim:
 1. A compound of Formula I.

wherein R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, cyclopropyl, OCF₃, or OCHF₂; R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, —OCHF₂, or OCF₃; provided that R² may not be H if R¹ is H; A¹ and A² are taken together with their attached nitrogen to form

A³ is H, —C₍₁₋₆₎alkyl,

—SO₂CH(CH₃)₂, —SO₂CH₃,

wherein said —C₍₁₋₆₎alkyl is optionally substituted with one —NH₂ group, one or two —OH groups, and may be additionally substituted with up to six fluorine atoms; A⁴ is —H, or —CH₃; A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₁₋₆₎alkyl,

wherein said —C₍₁₋₆₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms; and said —C₍₁₋₆₎alkyl is independently optionally substituted with one cyclobutyl, or up to two cyclopropyl groups; and pharmaceutically acceptable salts thereof.
 2. The compound of claim 1 wherein: A⁵ is —C₍₄₋₆₎cycloalkyl, —C₍₃₋₆₎alkyl,

wherein said —C₍₃₋₆₎alkyl and —C₍₄₋₆₎cycloalkyl are optionally substituted with up to three fluorine atoms; and pharmaceutically acceptable salts thereof.
 3. The compound of claim 2 wherein: R¹ is H, —C₍₁₋₃₎alkyl, —CHF₂, —CF₃, —CN, —OCH₃, —OCH₂CH₃, or cyclopropyl; R² is H, F, —CHF₂, —CF₃, —CN, —OCH₃, or —OCHF₂; provided that R² may not be H if R¹ is H; and pharmaceutically acceptable salts thereof.
 4. The compound of claim 3 selected from the group consisting of:

and pharmaceutically acceptable salts thereof.
 5. The compound of claim 3 selected from the group consisting of:

and pharmaceutically acceptable salts thereof.
 6. The compound of claim 3 selected from the group consisting of:

and pharmaceutically acceptable salts thereof.
 7. The compound of claim 3 selected from the group consisting of:


8. A pharmaceutical composition, comprising a compound of claim 1 and a pharmaceutically acceptable carrier.
 9. A method for treating or ameliorating a RORγt mediated inflammatory syndrome, disorder or disease selected from the group consisting of: inflammatory bowel diseases, rheumatoid arthritis, psoriasis, chronic obstructive pulmonary disorder, psoriatic arthritis, ankylosing spondylitis, neutrophilic asthma, steroid resistant asthma, multiple sclerosis, and systemic lupus erythematosus, comprising administering to a subject in need thereof an effective amount of a compound of claim
 1. 10. A method for treating or ameliorating a RORγt mediated inflammatory syndrome, disorder or disease selected from the group consisting of: depression and metabolic syndrome, comprising administering to a subject in need thereof an effective amount of a compound of claim
 1. 11. The method of claim 9, wherein the disease is psoriasis.
 12. The method of claim 9, wherein the disease is rheumatoid arthritis.
 13. The method of claim 9, wherein the inflammatory bowel disease is ulcerative colitis.
 14. The method of claim 9, wherein the inflammatory bowel disease is Crohn's disease.
 15. The method of claim 9, wherein the disease is multiple sclerosis.
 16. The method of claim 9, wherein the disease is neutrophilic asthma.
 17. The method of claim 9, wherein the disease is steroid resistant asthma.
 18. The method of claim 9, wherein the disease is psoriatic arthritis.
 19. The method of claim 9, wherein the disease is ankylosing spondylitis.
 20. The method of claim 9, wherein the disease is systemic lupus erythematosus.
 21. The method of claim 9, wherein the disease is chronic obstructive pulmonary disorder.
 22. The method of claim 10, wherein the disease is depression.
 23. The method of claim 10, wherein the disease is metabolic syndrome.
 24. A method of inhibiting production of interleukin-17, comprising administering to a subject in need thereof an effective amount of a compound of claim
 1. 